chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84804647148046472GGCCC10GENICheterozygous52622328
84804647148046472GGCC10GENICheterozygous53363488
84804653848046539GGT17GENIChomozygous52622330
84804654048046541AAC17GENIChomozygous52622332
84804728248047283GA52GENIChomozygous52622334
84804843548048436AAG24GENICpossibly homozygous52622336
84804878848048789GGAC18GENIChomozygous52622338
84804884948048850T-10GENIChomozygous52622340
84804906848049069TG17GENIChomozygous52622342
84804974548049747TT--21GENIChomozygous52622346
84804977348049774CT24GENIChomozygous52622348
84804985148049852CT24GENIChomozygous52622350
84804985248049853AG24GENIChomozygous52622352
84805025448050255GA27GENIChomozygous52622354
84805035648050357CT25GENIChomozygous52622356
84805064748050648GA26GENIChomozygous52622358
84805069348050694CA35GENIChomozygous52622360
84805081248050813TG26GENIChomozygous52622362
84805083348050834CT26GENIChomozygous52622364
84805087448050875AT26GENIChomozygous52622366
84805092448050925GA38GENIChomozygous52622368
84805124648051247GGC28GENIChomozygous52622370
84805213148052132GA29GENIChomozygous52622372
84805370348053704CT17GENIChomozygous52622374
84805373948053743AGTG----20GENICheterozygous53429649
84805397548053976TC23GENIChomozygous52622380
84805407248054073CA26GENIChomozygous52622382
84805441848054419GT26GENIChomozygous52622384
84805441948054420AT26GENIChomozygous52622386
84805454248054543CT15GENIChomozygous52622388
84805482448054825TTTG25GENIChomozygous52622390
84805514548055146TC22GENIChomozygous52622392
84805562948055630GA25GENIChomozygous52622394
84805564348055644CCCTTT23GENIChomozygous53429651
84805568048055681CCTTT31GENIChomozygous52622402
84805568148055682CCTTTCTTTTTTTTTTTT31GENIChomozygous53382652
84805687148056872GA23GENIChomozygous52622404
84805700548057006T-21GENIChomozygous52622406
84805724548057246CCA5GENIChomozygous52622410