chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1692685179268518CA18GENICpossibly homozygous47724767
1692712429271243AG23GENIChomozygous47264714
1692722039272204TC11GENIChomozygous47264716
1692722529272253GC14GENIChomozygous47264718
1692727519272752AG18GENIChomozygous47724777
1692745919274592GA20GENIChomozygous47724779
1692756009275601GA17GENIChomozygous47606733
1692756799275680AC16GENIChomozygous47264722
1692756909275691CT18GENICpossibly homozygous47606734
1692758949275895AAG11GENICpossibly homozygous47724781
1692761409276141CT22GENIChomozygous47606736
1692767419276742GA17GENICpossibly homozygous47724783