chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X134979757134979758GA15GENIChomozygous108583523
X134981589134981590AG25GENIChomozygous108583525
X134982744134982745GA14GENIChomozygous108583527
X134982996134982997CT21GENIChomozygous108583529
X134985807134985808AG21GENIChomozygous108509446
X134985854134985855TC11GENIChomozygous108509450
X134985856134985857CT11GENIChomozygous108583531
X134986095134986096TG17GENIChomozygous108583533
X134986315134986316CA27GENIChomozygous108583535
X134986647134986648CT16GENIChomozygous108583537
X134987222134987223GA12GENIChomozygous108583539
X134987436134987437CT13GENIChomozygous108583541
X134987729134987730AG20GENIChomozygous108583543
X134988424134988425GA22GENIChomozygous108509452
X134988565134988566AG6GENIChomozygous108509454
X134988975134988976AT8GENIChomozygous108530264
X134989203134989204TG21GENIChomozygous108509456
X134989609134989610GA31GENIChomozygous108509458
X134989776134989777GA17GENIChomozygous108583545
X134989810134989811CG4GENIChomozygous108509460
X134990923134990924CT20GENIChomozygous108509462
X134992223134992224TC23GENIChomozygous108583547