chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1246990039246990040CT17GENIChomozygous108602183
1246990046246990046C17GENIChomozygous127501282
1246990066246990066A16GENIChomozygous127501283
1246990076246990076CC15GENIChomozygous127501284
1246990079246990079C14GENIChomozygous127501285
1246990139246990140T14GENIChomozygous127501286
1246990140246990141AC14GENIChomozygous120493859
1246990149246990150A15GENIChomozygous127501287
1246990187246990188T14GENIChomozygous127501288
1246990195246990195T14GENIChomozygous127501289
1246990253246990254A12GENIChomozygous127501290
1246990607246990608C20GENIChomozygous127501293
1246990654246990655T20GENIChomozygous127501294
1246990692246990693T23GENIChomozygous127501295
1247003437247003438A3GENIChomozygous130218048
1247003773247003774AC1GENIChomozygous108602192
1247010450247010451CG17GENIChomozygous108602209
1247018590247018591GT14GENIChomozygous120476742
1247018590247018590T13GENIChomozygous127501308
1247020291247020292TC18GENIChomozygous108602245