chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84804647148046472GGCCC11GENICpossibly homozygous52622328
84804647148046472GGCC11GENICheterozygous53363488
84804653848046539GGT21GENIChomozygous52622330
84804654048046541AAC22GENIChomozygous52622332
84804728248047283GA26GENIChomozygous52622334
84804843548048436AAG16GENICpossibly homozygous52622336
84804878848048789GGAC25GENIChomozygous52622338
84804884948048850T-18GENIChomozygous52622340
84804906848049069TG11GENIChomozygous52622342
84804928448049285AAC2GENIChomozygous53382644
84804974548049747TT--24GENIChomozygous52622346
84804977348049774CT26GENIChomozygous52622348
84804985148049852CT24GENIChomozygous52622350
84804985248049853AG24GENIChomozygous52622352
84805025448050255GA22GENIChomozygous52622354
84805035648050357CT19GENIChomozygous52622356
84805064748050648GA26GENIChomozygous52622358
84805069348050694CA27GENIChomozygous52622360
84805081248050813TG23GENIChomozygous52622362
84805083348050834CT25GENIChomozygous52622364
84805087448050875AT28GENIChomozygous52622366
84805092448050925GA23GENIChomozygous52622368
84805124648051247GGC32GENIChomozygous52622370
84805213148052132GA21GENIChomozygous52622372
84805370348053704CT6GENIChomozygous52622374
84805397548053976TC38GENIChomozygous52622380
84805407248054073CA29GENIChomozygous52622382
84805441848054419GT28GENICpossibly homozygous52622384
84805441948054420AT29GENICpossibly homozygous52622386
84805454248054543CT28GENIChomozygous52622388
84805482448054825TTTG22GENIChomozygous52622390
84805514548055146TC22GENIChomozygous52622392
84805562948055630GA21GENIChomozygous52622394
84805568048055681CCTTT18GENIChomozygous52622402
84805568148055682CCTTTCTTTTTTTTTTTT18GENIChomozygous53382652
84805687148056872GA29GENIChomozygous52622404
84805700548057006T-20GENIChomozygous52622406
84805724548057246CCA9GENIChomozygous52622410
84805373948053743AGTG----10GENICheterozygous53429649
84805564348055644CCCTTT11GENIChomozygous53429651