chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175309226653092267CT18GENIChomozygous111063009
175309230953092310GC22GENIChomozygous111063010
175309244653092447CG21GENIChomozygous111063011
175309284353092844GA16GENIChomozygous111063012
175309305153093052AG28GENIChomozygous111063013
175309313653093137AG20GENIChomozygous111063014
175309339253093393AC8GENIChomozygous111063015
175309342553093426AG12GENIChomozygous111063016
175309355553093556TC22GENIChomozygous111063017
175309356953093570CT20GENIChomozygous111063018
175309361953093620CT26GENIChomozygous111063019
175309365553093656AG24GENIChomozygous111063020
175309393653093937CT19GENIChomozygous111063021
175309393753093938GA19GENIChomozygous111063022
175309417753094178AC21GENIChomozygous111063023
175309491953094920TA27GENIChomozygous111600482
175309529953095300GA25GENIChomozygous111063024
175309544153095442TC27GENIChomozygous111063025
175309591753095918CT25GENIChomozygous111063026
175309696853096969GA35GENIChomozygous111063027
175309702653097027CT28GENIChomozygous111063028
175309737653097377TC36GENIChomozygous111063029
175309783653097837CT25GENIChomozygous111063030
175309876253098763CT25GENIChomozygous111063032
175310036653100367AG32GENIChomozygous111063033
175309334453093344A10GENICheterozygous129458170
175309350453093505T18GENIChomozygous129458171
175309866353098663GC19GENIChomozygous129458173
175309420553094206AT20GENIChomozygous111246875
175309851453098515GA23GENIChomozygous111246877
175309471753094718CT22GENIChomozygous111415766
175309476253094763GC15GENIChomozygous119293260
175309477853094779CT14GENIChomozygous119293261
175309479753094798GA17GENIChomozygous119293262
175309483653094837CT16GENIChomozygous119293263
175309476953094770GA14GENIChomozygous111352328
175309836153098362T22GENIChomozygous131192491