chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140197863140197864AC7GENIChomozygous893238992
7140198000140198001AG9GENIChomozygous893238993
7140198221140198222TC16GENIChomozygous893238994
7140198651140198652GA21GENIChomozygous893238995
7140199063140199064TC21GENIChomozygous893238996
7140199295140199296GA5GENICheterozygous893238997
7140199309140199310GA5GENICheterozygous893238998
7140200178140200179GA6GENIChomozygous893238999
7140201052140201053GA10GENIChomozygous893239000
7140201486140201487CT16GENIChomozygous893239001
7140201506140201507CT4GENIChomozygous893239002
7140202164140202165GA13GENIChomozygous893239003
7140202173140202174CT13GENIChomozygous893239004
7140202437140202438CT19GENIChomozygous893239005
7140204183140204184CT19GENIChomozygous893239006
7140205578140205579TC4GENIChomozygous893239007
7140205579140205580GA4GENIChomozygous893239008
7140205999140206000CT4GENIChomozygous893239009
7140206291140206292AT16GENIChomozygous893239010
7140206633140206634CA6GENIChomozygous893239011
7140207204140207205CA13GENICheterozygous893239012
7140208108140208109TC8GENIChomozygous893239013
7140208147140208148GC8GENICheterozygous893239014
7140209031140209032TA20GENIChomozygous893239015
7140209665140209666GA12GENIChomozygous893239016
7140210094140210095TG21GENIChomozygous893239017
7140211709140211710CT20GENIChomozygous893239018
7140212484140212485TG7GENIChomozygous893239019