chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5117700757117700758CT24GENIChomozygous113976626
5117700771117700772AG21GENIChomozygous113976627
5117701651117701652CA27GENICpossibly homozygous113976628
5117702704117702705CT22GENIChomozygous113976629
5117704007117704008TA25GENIChomozygous113976630
5117704130117704131CT25GENIChomozygous113976631
5117704525117704526AG25GENIChomozygous113976632
5117705412117705413TC27GENIChomozygous113976633
5117705535117705536GA15GENIChomozygous113976634
5117705600117705601CA12GENIChomozygous113976635
5117706306117706307GA22GENIChomozygous113976636