chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5151179813151179814A19GENIChomozygous128258296
5151179822151179822CA20GENIChomozygous128258297
5151179830151179831T22GENIChomozygous128258298
5151179840151179841T23GENIChomozygous128258299
5151179851151179852T23GENIChomozygous128258300
5151179855151179856G23GENIChomozygous128258301
5151179862151179864TG23GENIChomozygous128258302
5151181666151181667AG24GENIChomozygous114056585
5151181671151181672GA25GENIChomozygous114056587
5151181676151181677GT23GENIChomozygous114056589
5151181677151181678GT23GENIChomozygous114056591
5151181684151181685GA21GENIChomozygous118937204
5151181686151181687AG21GENIChomozygous118937206
5151181688151181689AG21GENIChomozygous119087548
5151181694151181695T23GENIChomozygous128258303
5151181704151181705A21GENIChomozygous128258304
5151181707151181708AG21GENIChomozygous119087549
5151181733151181734G19GENIChomozygous128258305
5151181737151181738AC19GENIChomozygous114056593
5151181738151181739AT19GENIChomozygous114056595
5151181770151181771CG18GENIChomozygous114056597
5151181774151181775T17GENIChomozygous128258306
5151181784151181785TC16GENIChomozygous114056599
5151181794151181795AC16GENIChomozygous119258375
5151181790151181791AC16GENIChomozygous119258372
5151181791151181792AC16GENIChomozygous119258373
5151181792151181793AT16GENIChomozygous119258374
5151181798151181799CG15GENIChomozygous114155877
5151181801151181802TA13GENIChomozygous114056601
5151181822151181823TA16GENIChomozygous114155878
5151181827151181834AAAAAAA14GENIChomozygous128258307
5151184961151184962CG10GENICheterozygous114056603
5151185071151185117CTCTCTCTCTGTCTCTCTCTCTCTCTCTGGCTCTCTCTCTCACTCA13GENIChomozygous128258309
5151185229151185230CG14GENIChomozygous114056610
5151188332151188333TC30GENIChomozygous114056612