chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7109541216109541217TC69GENIChomozygous145634623
7109541393109541394CT53GENIChomozygous145634624
7109542535109542536CT61GENIChomozygous145634625
7109542842109542843C49GENIChomozygous137973718
7109544358109544359TC61GENIChomozygous145634626
7109545977109545978AT73GENIChomozygous145634627
7109545992109545993AT76GENIChomozygous145634628
7109544433109544434TA69GENIChomozygous138179426
7109546004109546005AC75GENIChomozygous138179427
7109546437109546438TG67GENIChomozygous145634629
7109546705109546706GC60GENIChomozygous145634630
7109546826109546827CT59GENIChomozygous145634631
7109550096109550097TG65GENIChomozygous138179429
7109550343109550343AAAC66GENIChomozygous137973719
7109551377109551378TC65GENIChomozygous145634632
7109551961109551962TG71GENIChomozygous145634633
7109551981109551982CT62GENIChomozygous145634634