chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96656950066569501AG13GENIChomozygous117369478
96656971566569716TG9GENIChomozygous117369480
96658149566581496TG17GENIChomozygous117369484
96658818066588181CG15GENIChomozygous117369488
96659009966590100AT2GENIChomozygous117783350
96659010166590102AC2GENIChomozygous117783351
96659059766590598CT14GENIChomozygous117369502
96659854766598548TC29GENIChomozygous117711053
96660031566600316GA14GENIChomozygous117369506
96660298766602988GA15GENICpossibly homozygous117369510
96660998666609987GT10GENIChomozygous117369516
96661404266614043TA2GENIChomozygous117808093
96661603466616035CT25GENIChomozygous117711077
96661796066617961AC24GENIChomozygous117711081
96662142566621426TC20GENIChomozygous117711083
96662142966621430CT20GENIChomozygous117550475
96662399466623995AG31GENIChomozygous117369526
96662836466628365CT32GENIChomozygous117711089
96663007166630072AC8GENIChomozygous117369562
96663855366638554TC37GENIChomozygous117369574
96663905766639058AT16GENICpossibly homozygous117581733
96664473266644733CA20GENIChomozygous117711091
96664956766649568CG28GENIChomozygous117711093
96665235466652355TG17GENIChomozygous117711095
96665632366656324GT20GENIChomozygous117783353
96665640966656410CA5GENIChomozygous117369606
96665658466656585CT17GENIChomozygous117369608
96666040966660410GA35GENIChomozygous117369614
96666547766665478TC25GENIChomozygous117369618
96667028166670282GA24GENIChomozygous117711101
96667623166676232GC16GENIChomozygous117369652
96668039066680391GC12GENIChomozygous117711103