chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124256265242562653AG9GENIChomozygous50209360
124256297442562975GA16GENIChomozygous50209361
124256297842562979CT16GENIChomozygous50209362
124256326642563267GA20GENIChomozygous50209364
124256333142563332TC17GENIChomozygous50209365
124256376342563764AT24GENIChomozygous50209366
124256399942564000AT26GENIChomozygous50209367
124256411642564117AAAAC14GENIChomozygous50209368
124256412942564131AA--11GENIChomozygous50209369
124256413542564136AC13GENICpossibly homozygous50544380
124256439242564393CCT5GENICheterozygous50209370
124256456142564562TC14GENIChomozygous50209371
124256458242564583CT10GENIChomozygous50209372
124256521842565219CCTTT2GENIChomozygous50544382
124256559242565593T-21GENICpossibly homozygous50209376
124256770142567702TC13GENIChomozygous50209383
124257006542570068TAG---19GENIChomozygous50383160
124257007442570075TC20GENIChomozygous50383161
124257221242572214TT--19GENIChomozygous50209389
124257244042572441AG22GENICpossibly homozygous50209390
124256605042566051AG22GENIChomozygous50564013
124257218442572185AAT25GENICpossibly homozygous50564019
124256513242565133CCGATATATATATATATA2GENIChomozygous50592241
124256623942566240TTTTTATTTA4GENIChomozygous50804655
124257219842572199AAT18GENIChomozygous50640223
124257459142574592CT35GENICpossibly homozygous50327632
124257627842576279AG35GENIChomozygous50804657