chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263449011263449012GT21GENIChomozygous109027024
1263449595263449596TA16GENIChomozygous109027025
1263450387263450388AG18GENIChomozygous108633075
1263451228263451231TGC10GENIChomozygous131267624
1263451566263451567AG19GENIChomozygous109027026
1263451751263451754AAG8GENIChomozygous132543174
1263452091263452098GCCATGG15GENIChomozygous132543175
1263452150263452151TG16GENIChomozygous109027027
1263452284263452284A21GENIChomozygous131267625
1263452587263452587TTTTAAACAACC8GENIChomozygous131267626
1263453135263453136AG8GENIChomozygous108633083
1263454812263454813GA21GENIChomozygous109027029
1263455081263455082GA11GENIChomozygous109027030
1263455588263455589AT19GENIChomozygous108633087
1263455726263455727AG23GENIChomozygous109027031
1263457421263457422CA19GENIChomozygous109027038
1263457693263457694GA22GENIChomozygous109027039
1263458131263458132TG22GENIChomozygous108633093
1263459229263459230GA21GENIChomozygous108633095
1263459232263459232A21GENIChomozygous127508012
1263459234263459235GC22GENIChomozygous108633097