chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182456030324560304GA34GENIChomozygous110582834
182456283624562837AG27GENICpossibly homozygous110582836
182456290824562909TC29GENICpossibly homozygous110582838
182456294024562941AT31GENIChomozygous110582840
182456302424563025GA30GENIChomozygous110629511
182456422424564225TA20GENIChomozygous110582842
182456464824564649CA36GENIChomozygous110582844
182456490524564906CA37GENIChomozygous110582846
182456507424565075AG30GENIChomozygous110582848
182456733224567333TC26GENICpossibly homozygous110582850
182456778724567788CT20GENIChomozygous110582852
182456853024568531AG35GENIChomozygous110582854
182456899324568994GA46GENICpossibly homozygous110629513
182456920424569205AG37GENIChomozygous110582856
182456986124569862TA14GENICpossibly homozygous110582858
182457047724570478CA26GENICpossibly homozygous110582860