chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120376174120376175GA29GENIChomozygous54084070
7120376255120376256GGTTTTTTGTTTTTTTTGTTTTTTT7GENICheterozygous55001596
7120376255120376256GGTTTTTTGTTTTTTTTGTTTTTTTTGTTTTTTT7GENICpossibly homozygous55001598
7120376272120376273GT12GENIChomozygous55001600
7120378180120378181AG28GENIChomozygous54084073
7120378764120378765GA39GENIChomozygous54084074
7120381116120381117TC38GENIChomozygous54084076
7120382502120382503CCT14GENICheterozygous55361799