chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84804647148046472GGCCC5GENICheterozygous52622328
84804647148046472GGCC5GENICheterozygous53363488
84804653848046539GGT12GENIChomozygous52622330
84804654048046541AAC12GENIChomozygous52622332
84804728248047283GA25GENIChomozygous52622334
84804843548048436AAG18GENICpossibly homozygous52622336
84804878848048789GGAC11GENIChomozygous52622338
84804884948048850T-7GENIChomozygous52622340
84804906848049069TG7GENIChomozygous52622342
84804974548049747TT--15GENIChomozygous52622346
84804977348049774CT16GENIChomozygous52622348
84804985148049852CT11GENIChomozygous52622350
84804985248049853AG11GENIChomozygous52622352
84805025448050255GA20GENIChomozygous52622354
84805035648050357CT12GENIChomozygous52622356
84805064748050648GA7GENIChomozygous52622358
84805069348050694CA13GENICpossibly homozygous52622360
84805081248050813TG7GENIChomozygous52622362
84805083348050834CT8GENIChomozygous52622364
84805087448050875AT9GENIChomozygous52622366
84805092448050925GA8GENIChomozygous52622368
84805124648051247GGC10GENIChomozygous52622370
84805213148052132GA17GENIChomozygous52622372
84805370348053704CT1GENIChomozygous52622374
84805397548053976TC6GENIChomozygous52622380
84805407248054073CA11GENIChomozygous52622382
84805441848054419GT10GENIChomozygous52622384
84805441948054420AT12GENIChomozygous52622386
84805454248054543CT14GENIChomozygous52622388
84805482448054825TTTG10GENIChomozygous52622390
84805514548055146TC15GENIChomozygous52622392
84805562948055630GA24GENIChomozygous52622394
84805568048055681CCTTT10GENIChomozygous52622402
84805568148055682CCTTTCTTTTTTTTTTTT10GENIChomozygous53382652
84805687148056872GA14GENIChomozygous52622404
84805700548057006T-17GENIChomozygous52622406
84805724548057246CCA9GENIChomozygous52622410
84805373948053743AGTG----5GENICheterozygous53429649
84805564348055644CCCTTT14GENIChomozygous53429651