chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152534024152534025CT39GENIChomozygous114354648
5152535582152535583GT21GENIChomozygous114354650
5152536075152536076GA34GENIChomozygous114354652
5152536220152536221GT34GENIChomozygous114354654
5152536686152536687CT42GENIChomozygous114354656
5152536816152536817CG32GENIChomozygous114354658
5152537312152537313AG26GENIChomozygous114354660
5152537379152537380AG30GENIChomozygous114354662
5152537514152537515GA21GENICpossibly homozygous114354664
5152538237152538238AG23GENIChomozygous114354666
5152538502152538503TG23GENIChomozygous114354668
5152538556152538557AG21GENIChomozygous114354670
5152538640152538641CT22GENIChomozygous114354672
5152538873152538874CT21GENIChomozygous114354674
5152538885152538886GT23GENIChomozygous114354676
5152539080152539081GA14GENIChomozygous114354678
5152539607152539608TC35GENIChomozygous114354680
5152539721152539722TG32GENIChomozygous114354682
5152539730152539731CT32GENIChomozygous114354684
5152540341152540342GA30GENICheterozygous114354686
5152540508152540509AG31GENIChomozygous114354688
5152542286152542287GC23GENIChomozygous114354690
5152542518152542519TG24GENIChomozygous114354692
5152543595152543596TC17GENIChomozygous114354694
5152543723152543724AG15GENIChomozygous114354696
5152544820152544821AT6GENIChomozygous114354698