chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1246989688246989688CCTGGCTGGCGTGCGCACGTACACACACACACACACACACACACACACACACACACACACACACACACACACATCTCATTCTGCGGGCCCTGACCATT5GENIChomozygous130621420
1246990039246990040CT29GENIChomozygous108602183
1246990046246990046C28GENIChomozygous127501282
1246990066246990066A28GENIChomozygous127501283
1246990076246990076CC28GENIChomozygous127501284
1246990079246990079C26GENIChomozygous127501285
1246990139246990140T20GENIChomozygous127501286
1246990140246990141AC20GENIChomozygous120493859
1246990149246990150A21GENIChomozygous127501287
1246990187246990188T17GENIChomozygous127501288
1246990195246990195T16GENIChomozygous127501289
1246990253246990254A14GENIChomozygous127501290
1246990311246990312A8GENIChomozygous127501291
1246990363246990364TA5GENIChomozygous120512597
1246990363246990363G6GENIChomozygous127501292
1246990607246990608C23GENIChomozygous127501293
1246990654246990655T21GENIChomozygous127501294
1246990692246990693T17GENIChomozygous127501295
1247018590247018591GT24GENIChomozygous120476742
1247018590247018590T24GENIChomozygous127501308
1247020291247020292TC17GENIChomozygous108602245