chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1246990039246990040CT28GENIChomozygous108602183
1246990046246990046C26GENIChomozygous127501282
1246990066246990066A32GENIChomozygous127501283
1246990076246990076CC34GENIChomozygous127501284
1246990079246990079C36GENIChomozygous127501285
1246990139246990140T41GENIChomozygous127501286
1246990140246990141AC41GENIChomozygous120493859
1246990149246990150A42GENIChomozygous127501287
1246990187246990188T53GENIChomozygous127501288
1246990195246990195T53GENIChomozygous127501289
1246990253246990254A7GENIChomozygous127501290
1246990311246990312A14GENIChomozygous127501291
1246990363246990364TA14GENIChomozygous120512597
1246990363246990363G14GENIChomozygous127501292
1246990607246990608C47GENIChomozygous127501293
1246990654246990655T49GENIChomozygous127501294
1246990692246990693T49GENIChomozygous127501295
1247010450247010451CG54GENICpossibly homozygous108602209
1247018590247018591GT45GENIChomozygous120476742
1247018590247018590T44GENIChomozygous127501308
1247020291247020292TC62GENIChomozygous108602245
1247004182247004183AG5GENICheterozygous109208960
1247003388247003388CA3GENICheterozygous131992713
1247003437247003438A1GENIChomozygous130218048