chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156998341156998342TC11GENIChomozygous71175626
5156999712156999713TC36GENICpossibly homozygous71175628
5157001539157001540AT33GENIChomozygous71175630
5157002347157002348TC14GENIChomozygous71175632
5157002855157002856TC29GENIChomozygous71175634
5157003741157003742TC28GENIChomozygous71175636
5157007249157007250CT14GENIChomozygous71175638
5157008772157008773TC21GENIChomozygous71175642
5157008773157008774TC20GENIChomozygous71175644
5157011489157011490AG19GENIChomozygous71175646
5157012069157012070TC17GENIChomozygous71175648
5157012352157012353GA33GENIChomozygous71175650
5157016998157016999GA25GENIChomozygous71175658
5157017454157017455AG27GENIChomozygous71175660
5157017505157017506CT33GENIChomozygous72692206
5157017506157017507TA33GENIChomozygous71175662
5157019029157019030CT30GENIChomozygous71470391
5157019113157019114AG19GENIChomozygous71175676
5157021592157021593GA19GENIChomozygous71175678
5157021880157021881CG25GENICpossibly homozygous71175680
5157022539157022540CT27GENIChomozygous71175682
5157022575157022576TC16GENIChomozygous71175684
5157022617157022618CT15GENIChomozygous71175686
5157023064157023065AG33GENIChomozygous71175688
5157023295157023296AG31GENICpossibly homozygous71175690