chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84804653848046539GGT11GENIChomozygous52622330
84804654048046541AAC11GENIChomozygous52622332
84804728248047283GA26GENIChomozygous52622334
84804843548048436AAG15GENIChomozygous52622336
84804878848048789GGAC17GENIChomozygous52622338
84804884948048850T-16GENIChomozygous52622340
84804906848049069TG17GENIChomozygous52622342
84804916048049161GA7GENIChomozygous52622344
84804974548049747TT--14GENIChomozygous52622346
84804977348049774CT17GENIChomozygous52622348
84804985148049852CT15GENIChomozygous52622350
84804985248049853AG15GENIChomozygous52622352
84805025448050255GA19GENIChomozygous52622354
84805035648050357CT10GENIChomozygous52622356
84805064748050648GA9GENIChomozygous52622358
84805069348050694CA14GENIChomozygous52622360
84805081248050813TG16GENIChomozygous52622362
84805083348050834CT11GENIChomozygous52622364
84805087448050875AT14GENIChomozygous52622366
84805092448050925GA12GENIChomozygous52622368
84805124648051247GGC18GENIChomozygous52622370
84805213148052132GA10GENIChomozygous52622372
84805397548053976TC10GENIChomozygous52622380
84805407248054073CA10GENIChomozygous52622382
84805441848054419GT17GENIChomozygous52622384
84805441948054420AT17GENIChomozygous52622386
84805454248054543CT17GENIChomozygous52622388
84805514548055146TC17GENIChomozygous52622392
84805562948055630GA10GENIChomozygous52622394
84805687148056872GA17GENIChomozygous52622404
84805700548057006T-15GENIChomozygous52622406
84805723048057231CA9GENIChomozygous52622408