\Region = TrES_Lyr1 \Variability_Filter = R \Reference = O'Donovan et al. 2006, ApJ, 651, 61 \ STARID = unique identification for star within dataset: TrES_Lyr1_Num \ RA = Right Ascension of star in decimal degrees (J2000) \ Dec = Declination of star in decimal degrees (J2000) \ Bmag = value of apparent B magnitude \ Vmag = value of apparent V magnitude \ Rmag = Median value of apparent R magntidue \ Rerr = Observational uncertainty on R magnitude \ LCfil = name of filter in which lightcurve was obtained \ Npts = Number of datapoints in lightcurve \ StartHJD = minimal value of Heliocentric Julian date in lightcurve \ EndHJD = maximum value of Heliocentric Julian date in lightcurve \ LCdisp = 1-sigma rms dispersion of lightcurve around median value of Rmag lightcurve \ LCchisq = chi-squared of lightcurve about median lightcurve value \ N5sig = number of lightcurves points beyond 5-sigma of lightcurve median value \ F5sig = fraction of lightcurves points beyond 5-sigma of lightcurve median value \ Public = Y/N keyword indicating if lightcurve data available to public \ Region = identifier for part of sky observed in survey \ References = refereed publication referring to technical details of survey | STARID | RA | Dec | Bmag | Vmag | Rmag | Rerr | LCfil | Npts | StartHJD | EndHJD | LCdisp | LCchisq | N5sig | F5sig | Public | Region | Reference1| | char | double | double | real | real | real | real | char | int | double | double | real | real | int | real | char | char | char | | | degrees | degrees | mag | mag | mag | mag | | | days | days | mag | | | | | | | | | | | null | null | | | | | | | | | | | | | | TrES_Lyr1_00001 281.55083 +44.13611 8.333 8.110 9.251 0.1348 R 11398 2453541.787548 2453616.734163 0.031 3459.74 37 0.0032 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00002 281.24000 +44.35917 8.856 8.361 9.407 0.1395 R 11398 2453541.787548 2453616.734163 0.031 3300.09 64 0.0056 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00003 281.57250 +44.15000 10.077 8.899 9.837 0.0981 R 11398 2453541.787548 2453616.734163 0.022 953.34 51 0.0045 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00004 289.15125 +49.71278 10.372 9.303 10.644 0.0370 R 4105 2453549.748065 2453611.951450 0.126 10953.81 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00005 287.89708 +49.77028 11.220 9.614 10.564 0.0244 R 3941 2453549.748065 2453611.951450 0.131 10560.23 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00006 281.19958 +44.96111 11.495 10.353 10.743 0.0590 R 2315 2453549.854946 2453603.974180 0.024 239.78 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00007 281.43083 +49.25222 10.686 9.483 10.703 0.0275 R 11398 2453541.787548 2453616.734163 0.093 7613.44 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00008 281.28500 +46.27778 9.963 9.457 10.822 0.1354 R 2252 2453549.936846 2453611.951450 0.014 81.77 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00009 281.67292 +44.68500 10.593 9.579 10.858 0.0220 R 4139 2453549.748065 2453611.951450 0.154 16196.63 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00010 282.70708 +44.26389 11.093 9.848 10.932 0.0574 R 2935 2453549.750601 2453611.951450 0.005 8.69 4 0.0014 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00011 285.91250 +44.47222 10.813 9.774 10.788 0.0374 R 11398 2453541.787548 2453616.734163 0.112 9088.75 4 0.0004 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00012 288.90958 +48.18111 11.605 9.885 10.972 0.0200 R 1591 2453549.748065 2453611.939518 0.022 167.63 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00013 288.29417 +44.94806 9.885 9.430 10.946 0.0346 R 11398 2453541.787548 2453616.734163 0.119 7639.06 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00014 282.40833 +44.13889 11.162 9.836 10.971 0.0445 R 3171 2453549.753380 2453611.951450 0.006 10.24 10 0.0032 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00015 282.69000 +44.38806 10.069 9.505 11.070 0.0202 R 2657 2453549.813244 2453611.951450 0.026 192.85 2 0.0008 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00016 288.15875 +49.21833 9.950 9.412 11.050 0.0244 R 2157 2453549.748065 2453611.951450 0.018 107.45 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00017 281.87583 +47.19944 11.093 9.772 11.041 0.0183 R 1763 2453549.784052 2453611.951450 0.040 537.28 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00018 288.33167 +46.47167 11.453 9.971 10.976 0.0277 R 11398 2453541.787548 2453616.734163 0.126 12581.39 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00019 285.29250 +46.54611 11.220 9.848 10.836 0.0613 R 11398 2453541.787548 2453616.734163 0.170 27311.13 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00020 289.06750 +47.09556 null null 11.029 0.0322 R 11398 2453541.787548 2453616.734163 0.117 7001.54 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00021 282.39042 +47.71083 10.294 9.611 10.812 0.0368 R 11398 2453541.787548 2453616.734163 0.125 11189.51 1 0.0001 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00022 287.44750 +47.94500 10.837 9.764 10.884 0.0372 R 11398 2453541.787548 2453616.734163 0.113 12506.65 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00023 280.94042 +48.28583 9.944 9.563 11.118 0.0181 R 3107 2453549.749338 2453611.951450 0.017 88.84 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00024 288.41500 +50.00000 11.079 9.844 11.127 0.0367 R 2906 2453549.748065 2453611.951450 0.042 469.17 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00025 281.61167 +45.42861 10.927 9.796 11.185 0.0189 R 2820 2453549.750601 2453611.948904 0.027 192.91 2 0.0007 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00026 287.87667 +49.77528 12.596 10.302 11.087 0.0358 R 3276 2453549.748065 2453611.951450 0.027 234.17 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00027 285.30083 +49.62194 12.092 10.263 11.115 0.0340 R 11398 2453541.787548 2453616.734163 0.118 7592.36 2 0.0002 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00028 281.28000 +45.06250 10.926 9.833 11.120 0.0226 R 3306 2453549.758461 2453611.951450 0.006 11.74 7 0.0021 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00029 289.06625 +48.83917 11.631 9.996 11.125 0.0232 R 3199 2453549.748065 2453611.939518 0.017 88.36 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00030 288.78333 +46.17361 null null 11.023 0.0243 R 11398 2453541.787548 2453616.734163 0.141 9393.99 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00031 288.98750 +44.51194 null null 11.123 0.0335 R 2951 2453549.748065 2453611.951450 0.006 11.18 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00032 284.96208 +46.98056 9.781 9.454 10.896 0.0823 R 11398 2453541.787548 2453616.734163 0.206 42317.20 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00033 289.80125 +49.21944 10.153 9.492 11.132 0.0489 R 4003 2453549.748065 2453611.951450 0.005 6.30 3 0.0007 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00034 283.62083 +48.65917 10.990 9.771 11.041 0.0385 R 11398 2453541.787548 2453616.734163 0.139 16215.41 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00035 280.91125 +49.69806 10.305 9.548 11.152 0.0213 R 4132 2453549.748065 2453611.951450 0.005 6.84 2 0.0005 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00036 281.51292 +48.52917 11.823 10.092 11.163 0.0153 R 2654 2453549.748065 2453611.951450 0.019 113.11 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00037 284.75625 +49.40722 10.968 9.827 10.952 0.0456 R 11398 2453541.787548 2453616.734163 0.112 10265.71 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00038 282.09542 +45.38944 11.460 10.046 11.177 0.0200 R 2940 2453549.763530 2453611.951450 0.005 6.40 4 0.0014 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00039 282.24792 +44.96056 11.750 10.145 11.199 0.0374 R 3293 2453549.749338 2453611.951450 0.006 9.39 8 0.0024 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00040 282.06667 +49.24139 11.409 10.035 11.019 0.0293 R 11398 2453541.787548 2453616.734163 0.127 8799.83 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00041 286.13292 +46.72639 11.288 9.932 11.188 0.0386 R 11398 2453541.787548 2453616.734163 0.172 21761.45 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00042 281.79917 +49.14944 10.241 9.702 11.213 0.0422 R 4010 2453549.748065 2453611.951450 0.005 6.95 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00043 289.04833 +45.33167 null null 11.211 0.0308 R 11398 2453541.787548 2453616.734163 0.068 3236.21 1 0.0001 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00044 280.95792 +48.32583 10.830 9.889 11.219 0.0169 R 3423 2453549.748065 2453611.951450 0.006 8.83 1 0.0003 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00045 287.66125 +44.54056 10.531 9.811 11.216 0.0251 R 11398 2453541.787548 2453616.734163 0.105 7526.58 2 0.0002 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00046 287.14417 +48.69472 10.936 10.528 11.225 0.1327 R 4148 2453549.748065 2453611.951450 0.003 2.08 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00047 284.64583 +49.10583 11.114 9.900 11.215 0.0316 R 11398 2453541.787548 2453616.734163 0.140 8760.82 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00048 281.85250 +44.80972 11.242 10.068 11.233 0.0366 R 3830 2453549.750601 2453611.951450 0.006 8.37 3 0.0008 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00049 288.17042 +46.40028 10.286 9.726 11.219 0.0383 R 11398 2453541.787548 2453616.734163 0.164 20776.30 1 0.0001 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00050 283.58167 +44.39972 11.246 10.119 11.235 0.0312 R 3494 2453549.749338 2453611.951450 0.005 6.96 1 0.0003 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00051 281.74583 +46.25556 11.070 10.016 11.031 0.0346 R 11398 2453541.787548 2453616.734163 0.133 10456.64 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00052 285.70125 +44.93944 11.369 10.003 11.000 0.0412 R 11398 2453541.787548 2453616.734163 0.138 10507.80 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00053 285.51917 +48.99722 10.271 9.674 11.242 0.0172 R 2426 2453549.748065 2453611.951450 0.006 8.49 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00054 288.38417 +48.65306 9.643 9.370 11.252 0.0158 R 3363 2453549.748065 2453611.950177 0.037 322.26 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00055 287.85792 +49.17222 10.043 9.648 11.251 0.0327 R 3974 2453549.748065 2453611.951450 0.005 6.49 1 0.0003 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00056 286.77500 +47.17778 10.146 9.663 11.106 0.0390 R 11398 2453541.787548 2453616.734163 0.140 11153.90 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00057 287.98542 +48.38194 11.122 9.890 11.168 0.0308 R 11398 2453541.787548 2453616.734163 0.155 9078.52 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00058 287.23458 +45.36056 11.023 9.984 11.064 0.0295 R 11398 2453541.787548 2453616.734163 0.135 9169.22 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00059 287.51792 +45.96306 11.527 10.261 11.263 0.0426 R 11398 2453541.787548 2453616.734163 0.154 18374.58 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00060 289.53042 +46.95722 11.445 10.023 11.271 0.0294 R 3043 2453549.748065 2453611.951450 0.006 9.67 1 0.0003 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00061 284.38708 +49.65611 11.677 10.128 11.275 0.0350 R 3477 2453549.748065 2453611.951450 0.006 8.62 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00062 284.40500 +49.48000 11.526 10.137 11.283 0.0144 R 3015 2453549.748065 2453611.951450 0.005 7.52 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00063 285.06833 +44.90861 12.062 10.320 11.041 0.0362 R 11398 2453541.787548 2453616.734163 0.150 11770.73 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00064 286.26792 +46.30611 9.654 9.485 11.022 0.0278 R 11398 2453541.787548 2453616.734163 0.139 11896.27 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00065 288.20042 +49.48083 10.375 9.728 11.291 0.0256 R 4108 2453549.748065 2453611.951450 0.005 6.09 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00066 289.24167 +44.17861 11.957 10.350 11.297 0.0164 R 4148 2453549.748065 2453611.951450 0.005 6.80 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00067 285.13583 +49.45611 11.494 11.137 11.217 0.0369 R 11398 2453541.787548 2453616.734163 0.167 10159.22 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00068 284.39167 +46.20472 12.373 10.514 11.539 0.0135 R 1846 2453549.754652 2453611.921694 0.023 124.91 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00069 287.29375 +49.06417 11.369 10.031 11.309 0.0394 R 3156 2453549.748065 2453611.951450 0.005 7.43 1 0.0003 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00070 286.79667 +46.26833 11.201 9.968 11.054 0.0411 R 11398 2453541.787548 2453616.734163 0.170 14469.90 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00071 287.22500 +47.12361 11.485 10.065 11.061 0.0263 R 11398 2453541.787548 2453616.734163 0.167 13489.38 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00072 281.71292 +47.02167 11.624 10.090 11.499 0.0297 R 3133 2453549.754652 2453611.946358 0.024 125.45 5 0.0016 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00073 283.75458 +47.27222 11.317 10.017 11.300 0.0422 R 11398 2453541.787548 2453616.734163 0.199 25952.13 1 0.0001 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00074 280.95042 +49.24833 null null 11.324 0.0350 R 4147 2453549.748065 2453611.951450 0.004 4.77 1 0.0002 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00075 284.15000 +44.84278 11.296 10.194 11.325 0.0406 R 2890 2453549.762269 2453611.951450 0.005 6.02 1 0.0003 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00076 288.72542 +47.69667 null null 11.325 0.0328 R 3437 2453549.748065 2453611.950177 0.005 6.59 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00077 287.69875 +49.81222 11.450 10.050 11.333 0.0345 R 4034 2453549.748065 2453611.951450 0.005 5.92 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00078 281.44000 +49.20722 11.170 10.082 11.338 0.0392 R 4148 2453549.748065 2453611.951450 0.004 4.67 2 0.0005 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00079 282.57708 +48.51417 11.300 10.142 11.339 0.0412 R 3415 2453549.748065 2453611.951450 0.005 5.41 2 0.0006 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00080 287.52250 +44.54528 10.608 9.890 11.339 0.0226 R 3478 2453549.748065 2453611.951450 0.007 11.11 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00081 283.74458 +46.20500 11.772 10.317 11.340 0.0171 R 2513 2453549.750601 2453611.951450 0.004 4.80 1 0.0004 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00082 283.68625 +49.69833 11.656 10.190 11.343 0.0366 R 3757 2453549.748065 2453611.951450 0.005 7.01 1 0.0003 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00083 285.89792 +44.41194 11.302 10.170 11.339 0.0290 R 11398 2453541.787548 2453616.734163 0.126 11448.86 2 0.0002 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00084 281.83458 +46.89889 9.712 9.496 11.347 0.0186 R 3320 2453549.748065 2453611.951450 0.005 6.58 1 0.0003 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00085 285.31875 +45.16889 11.684 10.205 11.331 0.0372 R 11398 2453541.787548 2453616.734163 0.189 26146.80 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00086 286.78667 +44.36528 11.308 10.140 11.350 0.0349 R 3600 2453549.748065 2453611.951450 0.007 12.06 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00087 284.01583 +46.28361 11.566 10.305 11.355 0.0176 R 2414 2453549.754652 2453611.951450 0.037 341.53 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00088 285.30208 +47.69722 11.142 10.030 11.066 0.0344 R 11398 2453541.787548 2453616.734163 0.150 16125.13 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00089 288.66417 +46.06889 null null 11.352 0.0295 R 2407 2453549.748065 2453611.951450 0.006 8.96 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00090 289.01375 +44.05417 11.548 10.828 11.353 0.0137 R 4148 2453549.748065 2453611.951450 0.004 4.59 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00091 289.00792 +49.41083 null null 11.356 0.0486 R 14793 2453541.787548 2453616.734163 0.090 3705.69 5 0.0003 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00092 281.16708 +45.83583 11.389 10.364 11.355 0.0490 R 3861 2453549.748065 2453611.951450 0.005 7.11 1 0.0003 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00093 287.98208 +48.21667 10.141 9.745 11.365 0.0400 R 3498 2453549.748065 2453611.951450 0.019 87.42 0 0.0000 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00094 288.81333 +46.24806 null null 11.362 0.0301 R 11398 2453541.787548 2453616.734163 0.066 2500.47 6 0.0005 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00095 281.25083 +45.54000 10.702 9.960 11.366 0.0236 R 3878 2453549.748065 2453611.951450 0.006 7.82 2 0.0005 Y TrES_Lyr1 O'Donovan et al. 2006, ApJ, 651, 61 TrES_Lyr1_00096 284.32333 +44.45972 11.199 10.140 11.368 0.0248 R 3263 2453549.749338 2453611.951450 0.006 7.46 2 0.0006 Y TrES_Lyr1 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