chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84804647148046472GGCCC2GENIChomozygous52622328
84804653848046539GGT3GENICheterozygous52622330
84804654048046541AAC4GENICheterozygous52622332
84804728248047283GA15GENIChomozygous52622334
84804843548048436AAG10GENIChomozygous52622336
84804878848048789GGAC7GENICheterozygous52622338
84804884948048850T-3GENIChomozygous52622340
84804906848049069TG15GENICpossibly homozygous52622342
84804974548049747TT--5GENIChomozygous52622346
84804977348049774CT4GENIChomozygous52622348
84805025448050255GA17GENICheterozygous52622354
84805035648050357CT24GENICpossibly homozygous52622356
84805064748050648GA4GENICheterozygous52622358
84805069348050694CA9GENIChomozygous52622360
84805081248050813TG11GENIChomozygous52622362
84805083348050834CT14GENICpossibly homozygous52622364
84805087448050875AT12GENICheterozygous52622366
84805092448050925GA12GENIChomozygous52622368
84805124648051247GGC14GENICheterozygous52622370
84805213148052132GA16GENICpossibly homozygous52622372
84805370348053704CT6GENIChomozygous52622374
84805397548053976TC8GENICpossibly homozygous52622380
84805407248054073CA5GENICheterozygous52622382
84805454248054543CT10GENICheterozygous52622388
84805482448054825TTTG6GENIChomozygous52622390
84805514548055146TC11GENIChomozygous52622392
84805562948055630GA11GENIChomozygous52622394
84805564348055644CCCTTT1GENIChomozygous53429651
84805687148056872GA22GENIChomozygous52622404
84805700548057006T-7GENIChomozygous52622406