chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1659959305995931AG21GENICpossibly homozygous47253781
1659974895997492GTT---9GENIChomozygous47253782
1659978685997869GA25GENIChomozygous47253783
1659980355998036AC14GENIChomozygous47253784
1659985535998554AATCCAGGTCTCT2GENICheterozygous47253785
1659989725998973GT9GENIChomozygous47253786
1660000956000096CT20GENIChomozygous47253796
1660007566000757TC31GENIChomozygous47253797
1660012706001271TC28GENICpossibly homozygous47253798
1660014326001433CT25GENIChomozygous47253799
1660058656005866AT20GENIChomozygous47253800
1660077516007752C-18GENIChomozygous47253805
1660088276008828TC23GENICpossibly homozygous47253808