chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1246989688246989688CCTGGCTGGCGTGCGCACGTACACACACACACACACACACACACACACACACACACACACACACACACACACATCTCATTCTGCGGGCCCTGACCATT7GENIChomozygous130621420
1246990039246990040CT34GENIChomozygous108602183
1246990046246990046C32GENIChomozygous127501282
1246990066246990066A31GENIChomozygous127501283
1246990076246990076CC30GENIChomozygous127501284
1246990079246990079C31GENIChomozygous127501285
1246990139246990140T32GENIChomozygous127501286
1246990140246990141AC32GENIChomozygous120493859
1246990149246990150A29GENIChomozygous127501287
1246990187246990188T29GENIChomozygous127501288
1246990195246990195T31GENIChomozygous127501289
1246990253246990254A27GENIChomozygous127501290
1246990311246990312A24GENIChomozygous127501291
1246990363246990364TA13GENIChomozygous120512597
1246990363246990363G14GENIChomozygous127501292
1246990607246990608C46GENIChomozygous127501293
1246990654246990655T43GENIChomozygous127501294
1246990692246990693T42GENIChomozygous127501295
1247003773247003774AC3GENIChomozygous108602192
1247018590247018591GT36GENIChomozygous120476742
1247018590247018590T35GENIChomozygous127501308
1247020291247020292TC55GENIChomozygous108602245