chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1225096998225096999TA4GENIChomozygous108556508
1225097145225097146AG12GENIChomozygous108556509
1225097441225097442CG23GENICpossibly homozygous108556510
1225097666225097667GA6GENIChomozygous108556511
1225098057225098058GA16GENIChomozygous108556512
1225098131225098132GA13GENIChomozygous108556513
1225098712225098713CG12GENIChomozygous108556514
1225100182225100183TC13GENIChomozygous108556515
1225102081225102082AG23GENIChomozygous108556517
1225103373225103374AG6GENIChomozygous108556518
1225104217225104218AG22GENIChomozygous108556519
1225104575225104576CT13GENIChomozygous108556520
1225105058225105059AG9GENIChomozygous108556521
1225105267225105268AT10GENIChomozygous125312937
1225105549225105550TC20GENIChomozygous108556522
1225105820225105821GA10GENIChomozygous108556523
1225106706225106707CG5GENICheterozygous108556524
1225113212225113213AG17GENIChomozygous108556528
1225113371225113372GA24GENIChomozygous108556529
1225113433225113434TC14GENIChomozygous108556530
1225113558225113559GA18GENIChomozygous108556531
1225113782225113783AG19GENIChomozygous108556532
1225114360225114361GA23GENIChomozygous108556533
1225114522225114523CT17GENIChomozygous108556534
1225114523225114524CA17GENIChomozygous108556535
1225115012225115013GC22GENIChomozygous108556536