chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4135711556135711557CG17GENIChomozygous56939067
4135711568135711569GA20GENICheterozygous57338439
4135711574135711575AG20GENICheterozygous56939068
4135711625135711627AG--9GENICpossibly homozygous56939072
4135711662135711663CG20GENICpossibly homozygous56939073
4135712585135712586GA38GENIChomozygous57338441
4135713257135713258CT10GENIChomozygous56939075
4135714639135714640GA26GENIChomozygous56939078
4135714675135714676GC24GENIChomozygous57338443
4135714791135714792CT27GENIChomozygous56939079
4135715451135715452CT8GENIChomozygous57338445
4135715920135715921GA25GENIChomozygous57338447
4135715926135715927TC25GENIChomozygous56939081
4135716097135716098CA27GENIChomozygous56939082
4135716661135716666CAGTT-----27GENIChomozygous57338449
4135717331135717332A-29GENIChomozygous57338451
4135719827135719828G-17GENIChomozygous57338453
4135719869135719870TC20GENIChomozygous57338455
4135720506135720507AAT23GENIChomozygous56939085
4135720510135720511TTA25GENIChomozygous57338457
4135720528135720534CGATCA------18GENIChomozygous57338459
4135720598135720599TC24GENIChomozygous57338461
4135720633135720634GA24GENIChomozygous57338463
4135720672135720673AG23GENIChomozygous57338465
4135720699135720700GA21GENIChomozygous57338467
4135720895135720896TC20GENIChomozygous57338469
4135721169135721170AG11GENIChomozygous57338471