chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189857798189857798T32GENIChomozygous131298273
2189858716189858717AG56GENIChomozygous110172125
2189858759189858760TC57GENIChomozygous134806635
2189859499189859500TC68GENIChomozygous110172127
2189860331189860332AG50GENIChomozygous110805135
2189860749189860749A26GENIChomozygous134800296
2189860932189860933TA42GENIChomozygous110172130
2189861071189861071A44GENIChomozygous127718060
2189864653189864654AG21GENIChomozygous110172136
2189869067189869068AT22GENIChomozygous121549660
2189869069189869070AT21GENIChomozygous121549661
2189869071189869072AT19GENIChomozygous121549662
2189869073189869074AT19GENIChomozygous121549663
2189869075189869076AT19GENIChomozygous133665276
2189869078189869079GA19GENIChomozygous134806636
2189869151189869151C44GENIChomozygous134800297
2189870778189870779AT19GENIChomozygous134806637
2189875021189875022TC49GENIChomozygous110172150
2189862815189862816GA54GENICpossibly homozygous125744539