chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1188037738188037739AC5GENIChomozygous109175012
1188041313188041314AG9GENIChomozygous108457870
1188042264188042265CG7GENIChomozygous108457876
1188042363188042364GA6GENIChomozygous108763266
1188042364188042365AG6GENIChomozygous120475037
1188042537188042538CT12GENIChomozygous108457878
1188044012188044013CT5GENIChomozygous120848690
1188067700188067701CT7GENICpossibly homozygous120912291
1188083275188083276GA7GENIChomozygous109175018
1188084170188084171GC4GENIChomozygous108458135
1188084179188084180GT4GENIChomozygous120475041
1188084180188084181GT4GENIChomozygous120488435
1188097195188097196TG5GENICheterozygous120912292