chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2250762815250762816AG58GENIChomozygous74535878
2250763451250763452GA63GENIChomozygous74535881
2250766307250766308AT60GENIChomozygous74535884
2250766441250766442GA69GENICpossibly homozygous74535887
2250767102250767103GC52GENIChomozygous74535890
2250768610250768611CT50GENIChomozygous74535893
2250770693250770694CA67GENIChomozygous74535896
2250771493250771494GA42GENIChomozygous74535899
2250773160250773161GT55GENIChomozygous74535902
2250775122250775123GA51GENIChomozygous74535905
2250776092250776093TC65GENIChomozygous74535908
2250779856250779857GA54GENIChomozygous74535914
2250780207250780208TG69GENICpossibly homozygous74535917
2250782121250782122GA32GENIChomozygous74535920
2250783037250783038AG64GENIChomozygous74535923