chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5156351312156351313GT16GENIChomozygous126206642
5156390000156390001GA3GENICheterozygous114159064
5156399990156399991AG13GENIChomozygous126206644
5156416698156416699CA8GENIChomozygous126218656
5156470333156470334CG6GENIChomozygous126206645
5156470368156470369CA12GENIChomozygous126206646
5156470372156470373CT13GENIChomozygous126206647
5156470402156470403CA16GENIChomozygous126206648
5156499531156499532AG21GENIChomozygous114068109
5156441470156441471TC3GENICheterozygous126292231
5156531481156531482GA4GENIChomozygous126206652
5156531531156531532GT13GENIChomozygous126206653
5156531587156531588AG4GENIChomozygous126206656
5156531624156531625AG9GENIChomozygous126206657
5156540936156540937AC5GENIChomozygous126206658
5156554613156554614CT10GENIChomozygous126206659
5156560031156560032TG13GENIChomozygous126206660