chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107615230176152302CT11GENIChomozygous51500179
107615259476152595TC11GENIChomozygous51500180
107615260176152602CT7GENIChomozygous53336235
107615351576153516CA24GENIChomozygous52568095
107615353376153534GA24GENIChomozygous52568098
107615428876154289CT28GENIChomozygous52568101
107615470676154707AG17GENIChomozygous51500184
107615479776154798TC19GENIChomozygous51500185
107615494976154950TTC20GENIChomozygous51500186
107615597276155973TG17GENIChomozygous51500192
107615641776156418AG21GENICpossibly homozygous51500193
107615655576156563TGTGTATA--------12GENIChomozygous53336239
107615690976156910AG20GENIChomozygous51500194
107615728076157281TTG19GENIChomozygous51500195
107615840376158404AC10GENIChomozygous51500198
107615902276159023T-18GENIChomozygous52568110
107615995076159951AG19GENIChomozygous51500205
107615995476159956AC--19GENIChomozygous52386894
107616057976160580CT16GENIChomozygous53529797
107616200976162010GA22GENIChomozygous53529798
107616241676162417GGTCTCTC11GENIChomozygous53529799
107616242076162421GC18GENIChomozygous53529800
107616253476162535GC25GENIChomozygous53336242
107616270376162704GT20GENIChomozygous51500217
107616278276162783AG24GENIChomozygous51500219
107616317576163176CT28GENIChomozygous52568117
107616325176163252TG25GENIChomozygous52568121
107616419876164199AG19GENIChomozygous53336243
107616468876164689GA17GENIChomozygous52568124
107616513476165135AG15GENIChomozygous51500224
107616576176165762TTA14GENIChomozygous51500225
107616579176165798ACACTCC-------9GENIChomozygous53336244
107616604976166053AAAC----7GENIChomozygous52967969
107616690576166906TC10GENIChomozygous51500228
107616745876167461TTC---19GENIChomozygous53336246
107616790676167907AC22GENIChomozygous51500232
107616793376167934GA25GENIChomozygous53529801
107616869776168698CT21GENIChomozygous53529802
107616907976169085TTTTCT------13GENIChomozygous53529803
107616934076169341GT18GENIChomozygous51500234
107616953176169532GA17GENIChomozygous52568130
107616962376169624TC17GENICpossibly homozygous53529804
107616996976169973ATGT----18GENIChomozygous51500238
107617033376170334GGA11GENIChomozygous51500242
107617033476170335CCG11GENIChomozygous51500243
107617048876170489GA22GENIChomozygous52568133
107617092676170927AC18GENIChomozygous53336252
107617242476172425CT18GENIChomozygous52568136
107617247376172474CG20GENIChomozygous52568139
107617368876173689CCT11GENIChomozygous51500247
107617388876173889TTGATTG14GENIChomozygous51500248
107617522076175221CT18GENIChomozygous53336256
107617684876176849CT15GENIChomozygous53529805
107617726276177263T-18GENIChomozygous51500253
107617751976177520TA16GENIChomozygous51500256
107617791476177915T-20GENIChomozygous53336257
107617819176178192AT18GENIChomozygous52568150
107617836376178364GA21GENIChomozygous51500257
107617839676178397AG19GENIChomozygous51500258
107617901276179013TG12GENIChomozygous51500259
107617904376179044CT10GENIChomozygous53336258
107617934476179345A-15GENIChomozygous53529806
107617942476179425AC11GENIChomozygous51500261
107617942776179428GT12GENIChomozygous51500262
107617946776179468GA14GENIChomozygous51500263
107617951576179516GA13GENIChomozygous51500264
107617955876179559CT18GENIChomozygous51500265
107617981876179821TAA---12GENIChomozygous51500266