chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124256265242562653AG2GENIChomozygous50209360
124256297442562975GA11GENIChomozygous50209361
124256297842562979CT11GENIChomozygous50209362
124256326642563267GA17GENIChomozygous50209364
124256333142563332TC21GENIChomozygous50209365
124256358642563588TC--11GENICheterozygous50599392
124256376342563764AT29GENIChomozygous50209366
124256399942564000AT20GENIChomozygous50209367
124256411642564117AAAAC18GENIChomozygous50209368
124256412942564131AA--18GENICpossibly homozygous50209369
124256413542564136AC21GENICpossibly homozygous50544380
124256456142564562TC11GENIChomozygous50209371
124256458242564583CT11GENIChomozygous50209372
124256513242565133CCGATATATATATATATA3GENIChomozygous50592241
124256521842565219CCTTT6GENIChomozygous50544382
124256559242565593T-18GENIChomozygous50209376
124256605042566051AG20GENIChomozygous50564013
124256623942566240TTTTTATTTA1GENIChomozygous50804655
124256763342567634T-5GENICheterozygous50544384
124256770142567702TC11GENIChomozygous50209383
124257006542570068TAG---13GENIChomozygous50383160
124257007442570075TC16GENIChomozygous50383161
124257218442572185AAT18GENIChomozygous50564019
124257219842572199AAT21GENIChomozygous50640223
124257221242572214TT--24GENIChomozygous50209389
124257244042572441AG15GENIChomozygous50209390
124257459142574592CT18GENIChomozygous50327632
124257627842576279AG11GENIChomozygous50804657