chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3131011278131011279C-5GENICheterozygous58696021
3131011820131011821GC8GENIChomozygous57677914
3131013356131013357AC1GENIChomozygous57677918
3131014014131014015CA6GENIChomozygous57677920
3131014235131014239CAGA----10GENIChomozygous57677922
3131015451131015452TC4GENIChomozygous57677926
3131015572131015573TC4GENIChomozygous57677928
3131015791131015792CT10GENIChomozygous57677930
3131016350131016351AG10GENIChomozygous57677932
3131016640131016641CCTTTT4GENICheterozygous58624065
3131016678131016679CT7GENIChomozygous57677934
3131016835131016836TC10GENIChomozygous57677936
3131017390131017391AT11GENIChomozygous57677938
3131017701131017702AG9GENIChomozygous57677940
3131017787131017788GGCT10GENIChomozygous57677942
3131017845131017846CT12GENIChomozygous57677943
3131018010131018011T-16GENIChomozygous57677945
3131018182131018183CA15GENIChomozygous57677947
3131019069131019070AG10GENIChomozygous57677949
3131019094131019095CT9GENIChomozygous57677951
3131019275131019276GA10GENIChomozygous57677953
3131020111131020112TC12GENIChomozygous57677957
3131020178131020179AC15GENIChomozygous57677959
3131020198131020199GA14GENIChomozygous57677961
3131020240131020241CT12GENIChomozygous57677963
3131020592131020596TTTT----12GENIChomozygous57677965
3131021119131021127TTGATTGA--------10GENICheterozygous59107492
3131021123131021127TTGA----10GENICpossibly homozygous58624066
3131022283131022284C-5GENIChomozygous57677969
3131022445131022446TC7GENIChomozygous57677971
3131022486131022487TC10GENIChomozygous57677973
3131022846131022851TGTGG-----5GENIChomozygous57677975
3131024554131024555AT11GENIChomozygous57677977
3131025138131025139GA7GENIChomozygous57677979