chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1239429727239429729TG46GENICheterozygous141084632
1239430132239430134CT17GENICheterozygous145126432
1239434068239434069AG54GENIChomozygous135845474
1239442695239442696CT39GENICpossibly homozygous140966672
1239442683239442684C40GENICheterozygous402982707
1239442683239442684CG40GENICpossibly homozygous402982708
1239476396239476397GA31GENICheterozygous402982711
1239476396239476397G31GENICheterozygous402982712
1239513854239513855T26GENICheterozygous402982714
1239475519239475520G13GENICheterozygous144530150
1239513854239513855TC26GENICpossibly homozygous402982715
1239543019239543020A48GENICpossibly homozygous402982716
1239543019239543020AG48GENICheterozygous402982717
1239543242239543243A38GENIChomozygous141180799
1239543242239543243AG38GENICheterozygous402982718
1239543418239543419AT44GENIChomozygous135845737
1239543548239543549TC31GENIChomozygous141304425
1239543293239543294TC45GENIChomozygous141304422
1239543494239543495GA34GENIChomozygous141304423
1239543522239543523TC36GENIChomozygous141304424
1239543557239543558TC34GENIChomozygous141304426
1239543580239543581AG39GENIChomozygous141304427
1239543584239543585AT39GENIChomozygous141304428
1239549099239549100GA51GENIChomozygous141304429
1239550020239550021TC64GENIChomozygous135845749
1239550032239550033TC64GENIChomozygous135845750
1239551300239551301GC51GENIChomozygous141304430