chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171224481612244817CG13GENIChomozygous47021992
171224482412244825GA11GENIChomozygous47021993
171224561312245614G-10GENIChomozygous47021994
171224564112245642GA14GENICpossibly homozygous47021995
171224580012245801AG5GENIChomozygous47021997
171224799512247996GA25GENICpossibly homozygous47366776
171224983112249832GGACT10GENICpossibly homozygous47022008
171225052612250527GC15GENICpossibly homozygous47022010
171225548912255490GA22GENICpossibly homozygous47366778
171225745812257459TC17GENIChomozygous47366780
171225771312257714TC20GENIChomozygous47022020
171225800012258001GT18GENIChomozygous47022023
171225806912258070CG19GENICpossibly homozygous47022024
171225807712258078CT13GENICpossibly homozygous47022025
171225809912258100GT13GENIChomozygous47022026
171225817912258180AG13GENIChomozygous47022027
171225823512258236CT8GENIChomozygous47022028
171225829012258291GC11GENIChomozygous47022029
171225903912259040GA13GENIChomozygous47022030
171225906912259070AG14GENICpossibly homozygous47022031
171225923812259239GA16GENIChomozygous47022032
171225941912259420GA21GENICpossibly homozygous47022038
171225948612259487CT15GENIChomozygous47022039
171225956612259567TC23GENIChomozygous47022040
171225974012259741TG18GENIChomozygous47022041
171225989612259897TC19GENIChomozygous47022042
171225997112259972AG22GENICpossibly homozygous47022043
171226001812260019GT12GENIChomozygous47022044
171226009512260096AG23GENICpossibly homozygous47022045
171226017912260180GT28GENICpossibly homozygous47022046
171226026912260270AG24GENICpossibly homozygous47022047
171226037812260379AG15GENIChomozygous47022048
171226048112260482GA15GENICpossibly homozygous47022049
171226088312260885GG--10GENIChomozygous47703012
171226089112260892GT11GENIChomozygous47703015
171226100412261005TC10GENICpossibly homozygous47022051