chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146056805560568056AT22GENIChomozygous113475328
146056834960568350AG24GENIChomozygous113475330
146056892860568929TA23GENIChomozygous113475332
146056997060569971GC17GENIChomozygous118699709
146057056360570564GC19GENIChomozygous113475334
146057254860572549TC28GENIChomozygous113475336
146057665460576655GA30GENIChomozygous113475338
146057819860578199AC21GENIChomozygous113475340
146057848060578481GT17GENIChomozygous113475342
146058039760580398CG21GENIChomozygous113475344
146058562460585625CT27GENIChomozygous113475346
146058697860586979GC30GENIChomozygous113475348
146058708260587083CG26GENICpossibly homozygous118699710
146058776560587766AG24GENIChomozygous113475350
146058787960587880GA35GENIChomozygous113475352
146059089860590899TC33GENIChomozygous113475354
146059287760592878AG22GENIChomozygous113475356