chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121371598613715987GC58INTERGENIChomozygous50281326
121371613413716135AG71INTERGENIChomozygous50281327
121371676613716767AG57INTERGENIChomozygous50281328
121371676913716770GA58INTERGENIChomozygous50281329
121371696313716964GT72INTERGENIChomozygous50281330
121371697713716978AC66INTERGENIChomozygous50281331
121371697813716979AC65INTERGENIChomozygous50062164
121371750713717518GACAACCAACA-----------12INTERGENIChomozygous50281332
121371752213717523GA20INTERGENIChomozygous50281333
121371757613717577GA42INTERGENICpossibly homozygous50281334
121371761613717617CT56INTERGENICpossibly homozygous50281335
121371773313717734CA11INTERGENIChomozygous50062166
121371813113718132TC46INTERGENICheterozygous50062186
121371815313718154TA30INTERGENICheterozygous50062189
121371816113718162GA24INTERGENICheterozygous50062191
121371819913718200AAT13INTERGENICheterozygous50062193
121371820113718202AAAAC12INTERGENICheterozygous50281336
121371820413718205GC12INTERGENICheterozygous50281337
121371821513718216CG6INTERGENICheterozygous50281338
121371822313718224GC6INTERGENICheterozygous50281339
121371868413718685CT50INTERGENIChomozygous50281340