chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124256297442562975GA7GENIChomozygous50209361
124256297842562979CT6GENIChomozygous50209362
124256324842563249CA15GENIChomozygous50209363
124256326642563267GA12GENIChomozygous50209364
124256333142563332TC16GENIChomozygous50209365
124256376342563764AT21GENICpossibly homozygous50209366
124256399942564000AT17GENIChomozygous50209367
124256439242564393CCT24GENIChomozygous50209370
124256456142564562TC14GENICpossibly homozygous50209371
124256458242564583CT15GENICheterozygous50209372
124256514742565148TTATCG2GENICheterozygous50209373
124256517042565171GA1GENIChomozygous50209374
124256559242565593T-5GENICheterozygous50209376
124256559742565603TTTTTC------5GENICheterozygous50209377
124256667942566680CA17GENIChomozygous50209380
124256673342566734TC14GENICpossibly homozygous50209381
124256739342567394GT13GENIChomozygous50209382
124256770142567702TC1GENIChomozygous50209383
124256776742567768CG8GENIChomozygous50209384
124256843242568433CA13GENIChomozygous50209385
124256867842568679GA20GENICpossibly homozygous50209386
124257218542572186T-2GENIChomozygous50209388
124257244042572441AG9GENICheterozygous50209390