chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53602596536025966TC10GENIChomozygous113742277
53602602936026037TGTGTGTT18GENIChomozygous131381109
53603052436030525GA19GENIChomozygous119148419
53603126036031261AG25GENIChomozygous113742331
53603376036033760A7GENIChomozygous128169017
53603589036035891CA16GENIChomozygous113742347
53603901936039020TG20GENIChomozygous119148423
53604757436047575AC16GENIChomozygous113742431
53603587536035876G14GENIChomozygous128169018
53603591836035919C12GENIChomozygous128169019
53604170636041706T19GENICpossibly homozygous131381110
53604752336047528TATGA14GENIChomozygous131381111
53604083236040833AT21GENIChomozygous119148425
53604585836045859TC18GENIChomozygous113742421
53604737636047377AG23GENIChomozygous113742429
53603376936033770CA7GENIChomozygous128283536
53603383536033836A5GENIChomozygous130309601
53603384036033841TG5GENIChomozygous130318609
53605163736051638GA21GENIChomozygous119148427
53605202136052022AT15GENIChomozygous113742451
53605343936053440C8GENIChomozygous130309602
53605279336052794AG19GENIChomozygous131397072