chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2257394960257394961GA51GENIChomozygous110411891
2257395461257395463AG26GENICheterozygous127768528
2257395504257395510GAGAGT21GENICheterozygous127768529
2257398404257398405CG68GENIChomozygous110411893
2257398613257398614CT46GENIChomozygous110411895
2257399081257399082A26GENIChomozygous127768530
2257399097257399097T23GENICpossibly homozygous127768531
2257401875257401876TA54GENIChomozygous110411897
2257403118257403119T47GENIChomozygous127768532
2257403607257403608AG55GENIChomozygous110411899
2257404394257404395TC81GENIChomozygous110411901
2257404608257404609GT68GENIChomozygous110411903
2257405158257405159GA52GENIChomozygous110411905
2257407378257407379CT64GENIChomozygous110411907
2257407718257407719CT52GENICpossibly homozygous110411909
2257409650257409651C51GENICpossibly homozygous127768533
2257409790257409791GA45GENIChomozygous110411911
2257413493257413494GA56GENIChomozygous110411915
2257413945257413946CT49GENIChomozygous110411917
2257414365257414366AC45GENIChomozygous110411919
2257414716257414717GA63GENICpossibly homozygous110411921
2257415716257415717TC62GENIChomozygous110411923
2257416164257416165AT58GENIChomozygous110411925
2257416398257416399GA51GENIChomozygous110411927
2257416869257416870TG68GENIChomozygous110411929
2257418739257418740AG59GENIChomozygous110411931
2257419128257419129GA65GENIChomozygous110411933
2257419578257419579TC100GENICheterozygous110411935
2257419989257419990GA73GENICheterozygous110411937
2257420036257420037GA89GENICheterozygous110411939
2257420137257420139AG86GENICheterozygous127768534
2257421359257421359C44GENICpossibly homozygous127768535
2257421769257421770AG54GENIChomozygous110411941