chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172149040921490410CT18GENIChomozygous939523998
172149156721491568GA27GENIChomozygous939523999
172149161721491618GA32GENIChomozygous939524000
172149191321491914GA17GENIChomozygous939524001
172149202121492022TC15GENIChomozygous939524002
172149230821492309AG21GENIChomozygous939524003
172149278521492786CT14GENIChomozygous939524004
172149306121493062CT20GENIChomozygous939524005
172149312621493127AG20GENIChomozygous939524006
172149312721493128GA20GENIChomozygous939524007
172149315521493156CT17GENIChomozygous939524008
172149360521493606GA24GENIChomozygous939524009
172149362321493624GA27GENIChomozygous939524010
172149363021493631TC24GENIChomozygous939524011
172149371021493711TC21GENIChomozygous939524012
172149373221493733GA19GENIChomozygous939524013
172149402121494022CG24GENIChomozygous939524014
172149432021494321TC25GENIChomozygous939524015
172149436621494367GA19GENIChomozygous939524016
172149484521494846CT16GENIChomozygous939524017
172149560921495610GT17GENIChomozygous939524018
172149605921496060CA27GENIChomozygous939524019
172149609021496091AG21GENIChomozygous939524020
172149621221496213AG25GENIChomozygous939524021
172149657721496578GT23GENIChomozygous939524022
172149685021496851CT16GENIChomozygous939524023
172149861821498619TC15GENIChomozygous939524024
172149864621498647TA11GENIChomozygous939524025
172149910921499110CT17GENIChomozygous939524026