chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84804647148046472GGCCC13GENICpossibly homozygous52622328
84804647148046472GGCC13GENICheterozygous53363488
84804653848046539GGT23GENIChomozygous52622330
84804654048046541AAC23GENIChomozygous52622332
84804728248047283GA33GENIChomozygous52622334
84804843548048436AAG28GENIChomozygous52622336
84804878848048789GGAC22GENIChomozygous52622338
84804884948048850T-21GENIChomozygous52622340
84804906848049069TG30GENIChomozygous52622342
84804928448049285AAC7GENICheterozygous53382644
84804974548049747TT--32GENIChomozygous52622346
84804977348049774CT39GENIChomozygous52622348
84804985148049852CT30GENIChomozygous52622350
84804985248049853AG30GENIChomozygous52622352
84805025448050255GA36GENIChomozygous52622354
84805035648050357CT29GENIChomozygous52622356
84805064748050648GA30GENIChomozygous52622358
84805069348050694CA28GENIChomozygous52622360
84805081248050813TG40GENIChomozygous52622362
84805083348050834CT38GENIChomozygous52622364
84805087448050875AT40GENIChomozygous52622366
84805092448050925GA29GENIChomozygous52622368
84805124648051247GGC33GENIChomozygous52622370
84805213148052132GA29GENIChomozygous52622372
84805370348053704CT21GENIChomozygous52622374
84805373948053743AGTG----31GENICheterozygous53429649
84805397548053976TC33GENIChomozygous52622380
84805407248054073CA31GENIChomozygous52622382
84805441848054419GT34GENIChomozygous52622384
84805441948054420AT34GENIChomozygous52622386
84805454248054543CT30GENIChomozygous52622388
84805482448054825TTTG30GENICpossibly homozygous52622390
84805514548055146TC37GENIChomozygous52622392
84805562948055630GA24GENIChomozygous52622394
84805564348055644CCCTTT15GENIChomozygous53429651
84805568048055681CCTTT11GENIChomozygous52622402
84805568148055682CCTTTCTTTTTTTTTTTT11GENIChomozygous53382652
84805687148056872GA18GENIChomozygous52622404
84805688748056888CT22GENIChomozygous53270584
84805700548057006T-22GENICpossibly homozygous52622406
84805724548057246CCA10GENIChomozygous52622410