chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1189433122189433123AG22GENIChomozygous108976673
1189434027189434028TC27GENIChomozygous108976675
1189434587189434588TG27GENIChomozygous108976676
1189434976189434977GT19GENIChomozygous108976677
1189435128189435129GA9GENIChomozygous108976678
1189435325189435326GA22GENIChomozygous108976679
1189435462189435463GA24GENIChomozygous108976680
1189436240189436241GA17GENIChomozygous108976681
1189436565189436566TC21GENIChomozygous108976682
1189436630189436631GA23GENIChomozygous108976683
1189437446189437447TC29GENIChomozygous108976684
1189438795189438796TC20GENIChomozygous108976685
1189439360189439361GA27GENIChomozygous108976686
1189440186189440187CT21GENIChomozygous108976687
1189440375189440376AG31GENIChomozygous108976688
1189440712189440713TC32GENIChomozygous108976689
1189441301189441302AG23GENIChomozygous108976690
1189441427189441428GA19GENIChomozygous108976691
1189442084189442085CA31GENIChomozygous108976692
1189442196189442197GA31GENIChomozygous108463939
1189442452189442453AG22GENIChomozygous108976693
1189442820189442821AG7GENIChomozygous108976694
1189442835189442836GA6GENIChomozygous108976695
1189444339189444340AG22GENIChomozygous108976696
1189445640189445641CA10GENIChomozygous109176163
1189447373189447374TC13GENIChomozygous108976700
1189447856189447857AG30GENIChomozygous108976702
1189448203189448204TA42GENIChomozygous109176165
1189448290189448291AG28GENIChomozygous109176167
1189449980189449981CT24GENIChomozygous109176169
1189451301189451302TC15GENIChomozygous108976709
1189451825189451826CT14GENIChomozygous109176171
1189453819189453820AC17GENIChomozygous109176173
1189454787189454788TC29GENIChomozygous109176175
1189455551189455552CT26GENIChomozygous108463943
1189456877189456878AG28GENIChomozygous108976719
1189457397189457398TA22GENIChomozygous109176177
1189457482189457483AG32GENIChomozygous108463944