chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1125213182125213183CA22GENIChomozygous891413071
1125213926125213927CT13GENIChomozygous891413072
1125214231125214232TC18GENIChomozygous891413073
1125214871125214872AG19GENIChomozygous891413074
1125214953125214954CT13GENIChomozygous891413075
1125215239125215240GA16GENIChomozygous891413076
1125217485125217486GA18GENIChomozygous891413077
1125218976125218977TC20GENIChomozygous891413078
1125221356125221357CT23GENIChomozygous891413079
1125224111125224112CT26GENIChomozygous891413080
1125224413125224414AG11GENIChomozygous891413081
1125226171125226172TC5GENIChomozygous891413082
1125226820125226821GA17GENIChomozygous891413083
1125226862125226863GA15GENIChomozygous891413084
1125226934125226935GA26GENIChomozygous891413085
1125226967125226968CT22GENIChomozygous891413086
1125227524125227525CA10GENIChomozygous891413087
1125227655125227656GA21GENIChomozygous891413088
1125228013125228014TC13GENIChomozygous891413089
1125228026125228027AC10GENIChomozygous891413090
1125228141125228142GT10GENIChomozygous891413091
1125228215125228216CT18GENIChomozygous891413092
1125228275125228276CG21GENIChomozygous891413093
1125228284125228285TA16GENIChomozygous891413094
1125228363125228364TC21GENIChomozygous891413095
1125228434125228435TC10GENIChomozygous891413096
1125228819125228820CT9GENIChomozygous891413097