chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
131375501513755016GT5GENIChomozygous786610012
131376199613761997AG13GENICheterozygous786610013
131376200513762006GT12GENICheterozygous786610014
131376202313762024AT11GENICheterozygous786610015
131376204213762043TC13GENICheterozygous786610016
131376204513762046TG13GENICheterozygous786610017
131376204813762049TC14GENICheterozygous786610018
131376206113762062AT14GENICheterozygous786610019
131376206913762070AT16GENICheterozygous786610020
131376207413762075AG15GENICheterozygous786610021
131376209013762091TC14GENICheterozygous786610022
131376210013762101AG12GENICheterozygous786610023
131376211413762115GT11GENICheterozygous786610024
131376212413762125GA12GENICheterozygous786610025
131376212813762129AC11GENICheterozygous786610026
131376219613762197AG7GENICheterozygous786610027
131376219913762200AT8GENICheterozygous786610028
131379226113792262CG40GENICheterozygous786610029
131379229413792295CA47GENICheterozygous786610030
131379923813799239GC35GENICheterozygous786610031
131379926713799268GA37GENICheterozygous786610032
131379930513799306GA36GENICheterozygous786610033
131381680813816809AC30GENICheterozygous786610034
131382029613820297TG76GENICheterozygous786610035