chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155691399155691400CT4GENIChomozygous114065394
5155694453155694454AT17GENIChomozygous114065396
5155696623155696624TC18GENIChomozygous114065400
5155698924155698925AT5GENIChomozygous126206498
5155699976155699977AG28GENIChomozygous114065402
5155704438155704439AG11GENIChomozygous114065404
5155705955155705956AT14GENIChomozygous114065405
5155707246155707247GA16GENIChomozygous114065407
5155707844155707845TA4GENICheterozygous126206499
5155707917155707918GA23GENIChomozygous114065409
5155708808155708809AG10GENIChomozygous114065411
5155709347155709348CT22GENIChomozygous114065413
5155709549155709550CT10GENIChomozygous114065415
5155710666155710667TC19GENIChomozygous114065417
5155712113155712114TC20GENIChomozygous114065419
5155712567155712568GA10GENIChomozygous114065421
5155716524155716525CT22GENIChomozygous114065423
5155717183155717184TC20GENIChomozygous114065425
5155717451155717452AG13GENIChomozygous114065427
5155719965155719966GA15GENIChomozygous114065433
5155721054155721055AT6GENIChomozygous126206500
5155723095155723096GA11GENIChomozygous114065435
5155723241155723242AG8GENIChomozygous114065437
5155724209155724210AG18GENIChomozygous114065439
5155724515155724516GT15GENIChomozygous114065441
5155727646155727647TC9GENIChomozygous114065443