chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214124348214124349AG5GENICheterozygous891544662
1214124388214124389CA6GENICheterozygous891544663
1214127746214127747GC16GENIChomozygous891544664
1214128734214128735CT10GENIChomozygous891544665
1214128881214128882CG7GENIChomozygous891544666
1214130010214130011GA22GENIChomozygous891544667
1214131357214131358AG19GENIChomozygous891544668
1214132307214132308GC4GENIChomozygous891544669
1214132380214132381AG18GENIChomozygous891544670
1214132530214132531CT14GENIChomozygous891544671
1214132768214132769CG14GENIChomozygous891544672
1214135782214135783AG10GENIChomozygous891544673
1214137707214137708CG5GENIChomozygous891544674
1214138264214138265GT15GENIChomozygous891544675
1214139070214139071CG4GENIChomozygous891544676
1214139461214139462AT9GENIChomozygous891544677
1214140827214140828GT12GENIChomozygous891544678
1214141343214141344AG11GENICheterozygous891544679
1214142890214142891AG16GENIChomozygous891544680
1214146027214146028TC12GENIChomozygous891544681
1214146950214146951GA18GENIChomozygous891544682