chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84804647148046472GGCC3GENIChomozygous53363488
84804653848046539GGT15GENIChomozygous52622330
84804654048046541AAC16GENIChomozygous52622332
84804728248047283GA24GENIChomozygous52622334
84804843548048436AAG21GENIChomozygous52622336
84804878848048789GGAC16GENIChomozygous52622338
84804884948048850T-12GENIChomozygous52622340
84804906848049069TG8GENIChomozygous52622342
84804974548049747TT--14GENIChomozygous52622346
84804977348049774CT13GENIChomozygous52622348
84804985148049852CT15GENIChomozygous52622350
84804985248049853AG14GENIChomozygous52622352
84805025448050255GA25GENIChomozygous52622354
84805035648050357CT19GENIChomozygous52622356
84805064748050648GA14GENIChomozygous52622358
84805069348050694CA12GENIChomozygous52622360
84805081248050813TG12GENIChomozygous52622362
84805083348050834CT12GENIChomozygous52622364
84805087448050875AT9GENIChomozygous52622366
84805092448050925GA9GENICpossibly homozygous52622368
84805124648051247GGC13GENIChomozygous52622370
84805213148052132GA23GENIChomozygous52622372
84805370348053704CT7GENIChomozygous52622374
84805373948053743AGTG----8GENICheterozygous53429649
84805397548053976TC11GENIChomozygous52622380
84805407248054073CA18GENIChomozygous52622382
84805441848054419GT18GENIChomozygous52622384
84805441948054420AT19GENIChomozygous52622386
84805454248054543CT21GENIChomozygous52622388
84805482448054825TTTG14GENICpossibly homozygous52622390
84805514548055146TC17GENIChomozygous52622392
84805562948055630GA19GENIChomozygous52622394
84805564348055644CCCTTT12GENIChomozygous53429651
84805568048055681CCTTT6GENIChomozygous52622402
84805568148055682CCTTTCTTTTTTTTTTTT6GENIChomozygous53382652
84805687148056872GA10GENIChomozygous52622404
84805700548057006T-17GENIChomozygous52622406
84805724548057246CCA1GENIChomozygous52622410