chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263450387263450388AG21GENIChomozygous108633075
1263452001263452002TA21GENICpossibly homozygous108633079
1263452452263452453GA21GENIChomozygous108633081
1263452695263452696T18GENIChomozygous135289863
1263453135263453136AG20GENIChomozygous108633083
1263459229263459230GA17GENIChomozygous108633095
1263459232263459232A17GENIChomozygous127508012
1263454270263454270T22GENIChomozygous127508009
1263455287263455288CT16GENIChomozygous135297639
1263459234263459235GC20GENIChomozygous108633097
1263459683263459684TC33GENIChomozygous109217072
1263481791263481792CT11GENIChomozygous108633187