chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1189433122189433123AG10GENIChomozygous108976673
1189433629189433630GA36GENIChomozygous108976674
1189434027189434028TC32GENIChomozygous108976675
1189434587189434588TG25GENIChomozygous108976676
1189434976189434977GT29GENIChomozygous108976677
1189435128189435129GA36GENIChomozygous108976678
1189435325189435326GA15GENIChomozygous108976679
1189435462189435463GA14GENIChomozygous108976680
1189436240189436241GA28GENIChomozygous108976681
1189436565189436566TC17GENIChomozygous108976682
1189436630189436631GA17GENIChomozygous108976683
1189437446189437447TC33GENIChomozygous108976684
1189438795189438796TC12GENIChomozygous108976685
1189439360189439361GA43GENIChomozygous108976686
1189440186189440187CT17GENIChomozygous108976687
1189440375189440376AG23GENIChomozygous108976688
1189440712189440713TC23GENIChomozygous108976689
1189441301189441302AG22GENIChomozygous108976690
1189441427189441428GA27GENIChomozygous108976691
1189442084189442085CA18GENIChomozygous108976692
1189442196189442197GA9GENIChomozygous108463939
1189442452189442453AG47GENIChomozygous108976693
1189442820189442821AG14GENIChomozygous108976694
1189442835189442836GA14GENIChomozygous108976695
1189444339189444340AG46GENIChomozygous108976696
1189445640189445641CA30GENIChomozygous109176163
1189447373189447374TC15GENIChomozygous108976700
1189447856189447857AG27GENIChomozygous108976702
1189448203189448204TA20GENIChomozygous109176165
1189448290189448291AG27GENIChomozygous109176167
1189449980189449981CT21GENIChomozygous109176169
1189451301189451302TC25GENIChomozygous108976709
1189451825189451826CT27GENIChomozygous109176171
1189453819189453820AC30GENIChomozygous109176173
1189454787189454788TC30GENIChomozygous109176175
1189455551189455552CT21GENIChomozygous108463943
1189456877189456878AG22GENIChomozygous108976719
1189457397189457398TA7GENIChomozygous109176177
1189457482189457483AG10GENIChomozygous108463944
1189457505189457506GA12GENIChomozygous109176179