chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186360297963602980AT22GENIChomozygous110484772
186361866063618662GT9GENICheterozygous131545799
186362189263621892G19GENIChomozygous129545808
186362421663624217G20GENICheterozygous131545800
186362902263629023C13GENIChomozygous129545810
186362902763629030ACC13GENIChomozygous129545811
186362904563629046CT15GENIChomozygous110381044
186362905163629052A15GENIChomozygous129545812
186362906063629060T14GENIChomozygous129545813
186362908563629086CA16GENIChomozygous110381046
186362910363629103T19GENIChomozygous129545814
186362913163629131T16GENIChomozygous129545815
186362914563629145T19GENIChomozygous129545816
186363134463631344ATA15GENIChomozygous129545817
186363134863631348T16GENIChomozygous129545818
186363135363631353T17GENIChomozygous129545819
186363136563631366G18GENIChomozygous129545820
186363136863631369G18GENIChomozygous129545821
186363138463631385T20GENIChomozygous129545822
186363138963631390C19GENIChomozygous129545823
186363921163639218GGACACT11GENIChomozygous129545826
186364217263642172T27GENICheterozygous129545830
186365256563652566TG13GENICheterozygous130476815