chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4210445791210445792AG25GENICpossibly homozygous57071432
4210446380210446381CT21GENIChomozygous57071433
4210446416210446417GA19GENICpossibly homozygous57071434
4210446948210446990TCCTTCCTTCCTTCCCTCCCCTTCCTTCCTTCCTTCCTTCCT------------------------------------------3GENICheterozygous58370110
4210447012210447013T-2GENIChomozygous57071439
4210448345210448346CT12GENIChomozygous57071440
4210448398210448399GGCCC1GENIChomozygous58410688
4210450441210450442CT21GENIChomozygous57071443
4210450494210450495GA25GENICpossibly homozygous57071444
4210450985210450986TA5GENICheterozygous57071445
4210452183210452184TA12GENIChomozygous57071446