chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175309226653092267CT14GENIChomozygous111063009
175309230953092310GC19GENIChomozygous111063010
175309244653092447CG17GENIChomozygous111063011
175309284353092844GA16GENIChomozygous111063012
175309305153093052AG21GENIChomozygous111063013
175309313653093137AG19GENIChomozygous111063014
175309339253093393AC16GENIChomozygous111063015
175309342553093426AG19GENIChomozygous111063016
175309355553093556TC20GENIChomozygous111063017
175309356953093570CT21GENIChomozygous111063018
175309361953093620CT26GENIChomozygous111063019
175309365553093656AG26GENIChomozygous111063020
175309393653093937CT20GENIChomozygous111063021
175309393753093938GA20GENIChomozygous111063022
175309417753094178AC18GENIChomozygous111063023
175309529953095300GA13GENIChomozygous111063024
175309544153095442TC10GENIChomozygous111063025
175309591753095918CT17GENIChomozygous111063026
175309696853096969GA16GENIChomozygous111063027
175309702653097027CT16GENIChomozygous111063028
175309737653097377TC15GENIChomozygous111063029
175309783653097837CT13GENIChomozygous111063030
175309876253098763CT12GENIChomozygous111063032
175310036653100367AG12GENIChomozygous111063033
175309420553094206AT21GENIChomozygous111246875
175309851453098515GA10GENIChomozygous111246877
175309471753094718CT16GENIChomozygous111415766
175309476253094763GC17GENIChomozygous119293260
175309477853094779CT19GENIChomozygous119293261
175309479753094798GA18GENIChomozygous119293262
175309483653094837CT20GENIChomozygous119293263
175309476953094770GA18GENIChomozygous111352328
175309491953094920TA22GENIChomozygous111600482
175309836153098362T17GENIChomozygous131192491
175309334453093344A8GENICpossibly homozygous129458170
175309350453093505T23GENIChomozygous129458171
175309866353098663GC14GENIChomozygous129458173