chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9113579737113579738GA16GENICheterozygous117427217
9113579766113579767CT15GENICheterozygous117427218
9113579767113579768CT16GENICheterozygous117427219
9113580265113580266GC16GENICheterozygous117427225
9113581328113581329C11GENIChomozygous128746397
9113585061113585061GCGGCA14GENIChomozygous128746398
9113580601113580602CT11GENIChomozygous117645420
9113585167113585168CT21GENIChomozygous117645421
9113587986113587987AG26GENIChomozygous117645422
9113588131113588132GA21GENIChomozygous117645423
9113590798113590799GA24GENIChomozygous117645424
9113590838113590839GA27GENIChomozygous117645425
9113591279113591279C14GENICpossibly homozygous128746399
9113591342113591343CT21GENIChomozygous117645426
9113591817113591818CT20GENIChomozygous117645427
9113592455113592455A15GENIChomozygous128746400
9113592821113592822TC15GENIChomozygous117427237
9113593424113593425CA17GENIChomozygous117645428
9113594349113594350CT8GENIChomozygous117645429
9113594383113594384TC6GENIChomozygous117645430
9113596280113596281GA21GENIChomozygous117645431
9113596836113596837TC11GENIChomozygous117645432
9113597008113597010TA14GENICheterozygous128746401
9113597415113597416CT7GENIChomozygous117427243