chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182743093727430938CT49GENIChomozygous110649216
182743108227431083AG69GENICpossibly homozygous110317103
182743566927435670TG57GENIChomozygous110649217
182743877827438779AC42GENIChomozygous110649218
182743974527439746CT51GENIChomozygous110649219
182744493427444935AC46GENIChomozygous110649220
182743326327433264A38GENICpossibly homozygous130603061
182743340127433402CG67GENIChomozygous110587964
182743726427437265AT59GENICpossibly homozygous110587968
182744671427446715AG70GENIChomozygous110587976
182743709327437094CG32GENICpossibly homozygous131547650
182744024227440243A48GENIChomozygous131541870
182744025627440256A42GENICpossibly homozygous131541871
182744614027446140C40GENIChomozygous131541872
182744462727444628A23GENIChomozygous131203667
182744577627445776GC18GENICheterozygous133319520
182744590827445909TC63GENIChomozygous110858487
182744701727447018GA30GENIChomozygous110649221
182744726227447263GA47GENIChomozygous110649222
182744917327449174TA58GENICpossibly homozygous110317113
182744986427449865GA63GENIChomozygous110649223
182745064927450650GA55GENIChomozygous110649224
182745164127451642A71GENIChomozygous131541873
182745242727452428AT55GENICpossibly homozygous110317115
182745243427452435GT55GENICpossibly homozygous110317117
182744757127447572AG32GENIChomozygous110680567