chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5117700757117700758CT25GENIChomozygous113976626
5117700771117700772AG20GENIChomozygous113976627
5117701651117701652CA32GENIChomozygous113976628
5117702704117702705CT41GENIChomozygous113976629
5117704130117704131CT13GENIChomozygous113976631
5117704525117704526AG45GENIChomozygous113976632
5117705412117705413TC33GENIChomozygous113976633
5117705535117705536GA37GENIChomozygous113976634
5117705600117705601CA42GENIChomozygous113976635
5117706306117706307GA32GENIChomozygous113976636