chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146056805560568056AT30GENIChomozygous113475328
146056834960568350AG65GENIChomozygous113475330
146056892860568929TA15GENIChomozygous113475332
146056997060569971GC49GENICpossibly homozygous118699709
146057056360570564GC54GENIChomozygous113475334
146057254860572549TC72GENIChomozygous113475336
146057665460576655GA51GENIChomozygous113475338
146057819860578199AC39GENIChomozygous113475340
146057848060578481GT61GENIChomozygous113475342
146058039760580398CG32GENIChomozygous113475344
146058562460585625CT33GENIChomozygous113475346
146058697860586979GC53GENIChomozygous113475348
146058708260587083CG51GENICheterozygous118699710
146058776560587766AG43GENIChomozygous113475350
146058787960587880GA56GENIChomozygous113475352
146059089860590899TC54GENIChomozygous113475354
146059287760592878AG29GENIChomozygous113475356