chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48702799587027996CA21GENIChomozygous112767196
48702989687029897AG14GENIChomozygous112767202
48703074287030743GT24GENIChomozygous113130223
48703396687033967GA25GENIChomozygous112767206
48703469087034691GA17GENIChomozygous112767208
48703495387034954CG19GENIChomozygous112767210
48703569087035691CT22GENIChomozygous112767216
48703447387034474GT28GENIChomozygous113358301
48703449387034494CT31GENIChomozygous119585215
48703450187034502CT32GENICpossibly homozygous119585216
48704171187041712GT26GENICpossibly homozygous113280949
48704188387041884GA21GENIChomozygous119585217
48704214587042146CT22GENICpossibly homozygous119585218
48704485487044855GA10GENIChomozygous119585219
48705025787050258AC24GENIChomozygous119585220
48705040487050405CT24GENIChomozygous113130234
48705260687052607GA12GENIChomozygous119585221
48705289787052898AG24GENIChomozygous112767268
48705563187055632GA20GENIChomozygous112767278
48705853387058534TC26GENIChomozygous112767286
48705869687058697GA30GENIChomozygous112767288
48706457587064576CT20GENIChomozygous112767300