chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84804647148046472GGCCC1GENIChomozygous52622328
84804653848046539GGT12GENIChomozygous52622330
84804654048046541AAC12GENIChomozygous52622332
84804728248047283GA32GENIChomozygous52622334
84804843548048436AAG17GENIChomozygous52622336
84804878848048789GGAC26GENIChomozygous52622338
84804884948048850T-20GENIChomozygous52622340
84804906848049069TG24GENIChomozygous52622342
84804974548049747TT--24GENIChomozygous52622346
84804977348049774CT21GENIChomozygous52622348
84804985148049852CT27GENIChomozygous52622350
84804985248049853AG27GENIChomozygous52622352
84805025448050255GA23GENIChomozygous52622354
84805035648050357CT25GENIChomozygous52622356
84805064748050648GA25GENIChomozygous52622358
84805069348050694CA32GENIChomozygous52622360
84805081248050813TG23GENIChomozygous52622362
84805083348050834CT24GENICpossibly homozygous52622364
84805087448050875AT31GENIChomozygous52622366
84805092448050925GA27GENIChomozygous52622368
84805124648051247GGC20GENIChomozygous52622370
84805213148052132GA37GENIChomozygous52622372
84805370348053704CT13GENIChomozygous52622374
84805373948053743AGTG----9GENICheterozygous53429649
84805397548053976TC25GENIChomozygous52622380
84805407248054073CA30GENICpossibly homozygous52622382
84805441848054419GT16GENIChomozygous52622384
84805441948054420AT17GENIChomozygous52622386
84805454248054543CT23GENIChomozygous52622388
84805482448054825TTTG19GENIChomozygous52622390
84805514548055146TC20GENIChomozygous52622392
84805562948055630GA26GENIChomozygous52622394
84805564348055644CCCTTT18GENIChomozygous53429651
84805568048055681CCTTT18GENIChomozygous52622402
84805568148055682CCTTTCTTTTTTTTTTTT18GENIChomozygous53382652
84805687148056872GA20GENIChomozygous52622404
84805700548057006T-25GENICpossibly homozygous52622406
84805724548057246CCA6GENIChomozygous52622410