chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156998341156998342TC9GENIChomozygous71175626
5156999712156999713TC4GENIChomozygous71175628
5156999931156999932CG5GENIChomozygous73002052
5157001539157001540AT22GENIChomozygous71175630
5157002347157002348TC6GENIChomozygous71175632
5157002855157002856TC22GENIChomozygous71175634
5157003741157003742TC22GENIChomozygous71175636
5157008260157008261CA3GENIChomozygous73002055
5157008773157008774TC7GENIChomozygous71175644
5157012069157012070TC24GENIChomozygous71175648
5157012352157012353GA21GENIChomozygous71175650
5157016006157016007CT21GENIChomozygous71175654
5157016094157016095CG11GENIChomozygous71175656
5157016998157016999GA17GENIChomozygous71175658
5157017454157017455AG17GENIChomozygous71175660
5157017506157017507TA10GENIChomozygous71175662
5157019113157019114AG14GENIChomozygous71175676
5157021592157021593GA5GENIChomozygous71175678
5157021880157021881CG35GENIChomozygous71175680
5157022539157022540CT12GENIChomozygous71175682
5157022575157022576TC14GENIChomozygous71175684
5157022617157022618CT17GENIChomozygous71175686
5157023064157023065AG8GENIChomozygous71175688
5157023295157023296AG18GENIChomozygous71175690
5157017505157017506CT9GENIChomozygous72692206