chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155691399155691400CT26GENIChomozygous114065394
5155694453155694454AT59GENIChomozygous114065396
5155695875155695876CA35GENICheterozygous114065398
5155696623155696624TC38GENIChomozygous114065400
5155699976155699977AG33GENIChomozygous114065402
5155704438155704439AG29GENIChomozygous114065404
5155705955155705956AT59GENIChomozygous114065405
5155707246155707247GA32GENIChomozygous114065407
5155707917155707918GA60GENIChomozygous114065409
5155708808155708809AG29GENIChomozygous114065411
5155709347155709348CT53GENIChomozygous114065413
5155709549155709550CT51GENIChomozygous114065415
5155710666155710667TC34GENIChomozygous114065417
5155712113155712114TC26GENIChomozygous114065419
5155712567155712568GA65GENIChomozygous114065421
5155716524155716525CT29GENIChomozygous114065423
5155717183155717184TC55GENICpossibly homozygous114065425
5155717451155717452AG52GENIChomozygous114065427
5155717882155717883AC47GENIChomozygous114065429
5155718094155718095GC43GENIChomozygous114065431
5155719965155719966GA42GENIChomozygous114065433
5155723241155723242AG24GENIChomozygous114065437
5155724209155724210AG35GENIChomozygous114065439
5155724515155724516GT37GENIChomozygous114065441
5155727646155727647TC33GENIChomozygous114065443