chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1226976832226976833CT22GENIChomozygous108998577
1226977270226977271GA15GENIChomozygous108998578
1226977389226977390TC20GENICpossibly homozygous108998579
1226979733226979734CT28GENIChomozygous108998580
1226981679226981680GA23GENIChomozygous108998581
1226982031226982032CT26GENIChomozygous108998582
1226983197226983198GA22GENIChomozygous108998583
1226984410226984411GA30GENIChomozygous108998584
1226985572226985573AT21GENIChomozygous108998585
1226985923226985924TC24GENICheterozygous108998586
1226985927226985928TC25GENICheterozygous108998587
1226985931226985932TC25GENICpossibly homozygous108998588
1226986081226986082GC26GENIChomozygous108998589
1226986289226986290CT26GENIChomozygous108998590
1226986463226986464TC27GENIChomozygous108998591
1226986533226986534AG22GENIChomozygous108998592
1226987423226987424AG25GENIChomozygous108998593
1226987756226987757TC28GENIChomozygous108998594
1226988554226988555TC21GENIChomozygous108998595
1226988622226988623CG27GENIChomozygous108998596
1226990504226990505CT24GENIChomozygous108998597
1226991161226991162GA20GENIChomozygous108998598
1226991290226991291TC19GENIChomozygous108998599
1226992745226992746TA24GENIChomozygous108998600