chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146994545169945452A-11GENIChomozygous698525010
146994691669946917AG20GENIChomozygous547939340
146994904569949046CA12GENICpossibly homozygous547939341
146995168369951684GGA1GENIChomozygous698525011
146995175469951755AAGG5GENIChomozygous698525012
146995241569952416TG4GENIChomozygous547939342
146995375669953757AG19GENICpossibly homozygous547939343
146995428369954284CT5GENIChomozygous547939344
146995536469955365GT12GENICpossibly homozygous547939345
146995631869956319AAGGT7GENICpossibly homozygous698525013
146995811769958118AC1GENIChomozygous547939346
146995896369958964CT1GENIChomozygous547939347
146995966469959665AC13GENIChomozygous547939348
146995996669959967CT19GENICpossibly homozygous547939349
146996195569961956GA17GENIChomozygous547939350
146996285869962859CT2GENIChomozygous547939351
146997052269970523GA20GENICpossibly homozygous547939352