chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162685946426859465TG39GENIChomozygous111769726
162686002026860021TC33GENICpossibly homozygous112259343
162686175626861757GA25GENIChomozygous111769728
162686290626862907CT17GENIChomozygous112152885
162686388626863887AC23GENIChomozygous111769730
162686658626866587GA19GENIChomozygous111769732
162686682726866828A2GENIChomozygous129345766
162686697626866977GC11GENIChomozygous119104708
162686875626868757TC17GENIChomozygous111769734
162686989626869897CT27GENIChomozygous111769736
162686994826869949CG28GENIChomozygous111769738
162686998326869984CA35GENIChomozygous111769740
162687004426870045GA47GENIChomozygous111769742
162687037426870375CT27GENIChomozygous111769744
162687108026871081CT26GENIChomozygous111769746
162687181826871819CA18GENIChomozygous111769748
162687252626872528CA18GENIChomozygous129345767
162687259026872591TG25GENIChomozygous111769750
162687292826872928AC16GENICpossibly homozygous129345768
162687316926873170TC32GENIChomozygous111769752
162687423626874237AG24GENIChomozygous111769754
162687426126874262TC28GENIChomozygous111769756
162687435526874356TC28GENIChomozygous111769758
162687466126874662TC24GENIChomozygous111769760
162687467026874671C25GENIChomozygous129345769
162687580226875803GA28GENIChomozygous111769762