chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1157704713157704714TC17GENIChomozygous60909142
1157704779157704780CT26GENIChomozygous61544465
1157704963157704964TG24GENIChomozygous61544466
1157705139157705140TC24GENIChomozygous61544467
1157705257157705258TA35GENIChomozygous61544468
1157705336157705337CT22GENIChomozygous61544469
1157705337157705338CT21GENIChomozygous61544470
1157705749157705750CT26GENIChomozygous61544471
1157705933157705934CA27GENIChomozygous61544472
1157706114157706115CT21GENIChomozygous61544473
1157706222157706223GT21GENIChomozygous61544474
1157706500157706503GAA---16GENICpossibly homozygous60909144
1157707010157707011TG9GENICheterozygous61308153
1157707035157707036GA8GENICheterozygous61544475
1157707061157707062GA11GENICheterozygous61544476
1157707117157707120AAA---8GENIChomozygous61544477
1157707137157707145TGTTACAT--------10GENIChomozygous61544478
1157707321157707322AG21GENIChomozygous61544479
1157707339157707340TG23GENIChomozygous61544480
1157707893157707894AC29GENIChomozygous61544481
1157708142157708143CT18GENIChomozygous61544482
1157708157157708158A-17GENIChomozygous61544483
1157708169157708170GGAA21GENIChomozygous61544484
1157708392157708393AG38GENIChomozygous61544485
1157708499157708500T-33GENIChomozygous61544486
1157708632157708633GC29GENIChomozygous60909148