chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4210445791210445792AG24GENIChomozygous57071432
4210446380210446381CT21GENIChomozygous57071433
4210446416210446417GA20GENIChomozygous57071434
4210446948210446990TCCTTCCTTCCTTCCCTCCCCTTCCTTCCTTCCTTCCTTCCT------------------------------------------23GENIChomozygous58370110
4210447012210447013T-10GENICpossibly homozygous57071439
4210447680210447681TTTGTGTGTGTGTGTGTG1GENIChomozygous58410687
4210448345210448346CT17GENIChomozygous57071440
4210450150210450151GGCATCCATCCATC18GENICheterozygous58410689
4210450150210450151GGCATCCATCCATCCATC18GENICpossibly homozygous58370114
4210450441210450442CT31GENIChomozygous57071443
4210450494210450495GA33GENIChomozygous57071444
4210450985210450986TA24GENIChomozygous57071445
4210452183210452184TA16GENIChomozygous57071446
4210448398210448399GGCC3GENIChomozygous57611051