chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124810587448105875TC15GENIChomozygous115345490
124810643748106438AG15GENIChomozygous115345492
124810648748106487G13GENIChomozygous128998459
124810691648106917AG17GENIChomozygous115345494
124810692848106929CT17GENIChomozygous115345496
124810758848107589GA12GENIChomozygous115345498
124810982948109830AC19GENIChomozygous115345500
124811095048110951GT13GENIChomozygous115345502
124811102748111028GC18GENIChomozygous115345504
124811296548112966TC12GENIChomozygous115345506
124811457048114571CT18GENIChomozygous115345508
124811466948114670GA19GENIChomozygous115345510
124811655548116556GA12GENIChomozygous115345512
124811710848117109CA21GENIChomozygous115345514
124811914548119146GA11GENIChomozygous115345516
124812111848121119AT15GENIChomozygous115345518
124811741248117413GA6GENICheterozygous118272944