chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6136504517136504523GTGTGT------8GENIChomozygous56472021
6136505938136505939CG23GENIChomozygous56503839
6136509203136509204AG36GENIChomozygous54744962
6136510730136510731TC24GENIChomozygous54744964
6136511718136511732TGTGTGTGTGTGTG--------------4GENICheterozygous55542722
6136512548136512549AG25GENIChomozygous54744973
6136513252136513253AG25GENICpossibly homozygous54744979
6136513632136513633TTATA31GENIChomozygous54744986
6136514389136514390AATGTTTGTTTGTTTGTT17GENIChomozygous56503840
6136515053136515054AAGAAT14GENIChomozygous54744998
6136516405136516406GA34GENIChomozygous56503841
6136516938136516939AC23GENIChomozygous54745015
6136517529136517530TC18GENIChomozygous56503842
6136517551136517552AG23GENIChomozygous54745022
6136517875136517876GA29GENICpossibly homozygous54745025
6136517921136517926AAAAA-----7GENICheterozygous56503843
6136518000136518016GGGATCACTTACAGCA----------------23GENIChomozygous56503844
6136518041136518042AT25GENIChomozygous54745027
6136518360136518361GT36GENIChomozygous54745033
6136518362136518363AG37GENIChomozygous54745035
6136518955136518956GA33GENIChomozygous54745040
6136518960136518961AG33GENIChomozygous54745042
6136519094136519095TC24GENICpossibly homozygous56503845
6136519130136519131AG21GENICpossibly homozygous54745046
6136519153136519154TC19GENIChomozygous54745050
6136519326136519327TC24GENIChomozygous54745052
6136519407136519408AG19GENIChomozygous54745054
6136520073136520074TTC21GENIChomozygous54745056
6136520129136520130AT25GENIChomozygous54745058
6136520314136520315GA23GENIChomozygous56503846
6136520705136520706AC29GENIChomozygous54745064
6136520859136520860AC28GENIChomozygous54745066
6136521069136521070TC24GENIChomozygous54745068
6136521094136521095CT28GENIChomozygous56503847
6136521528136521529AG32GENIChomozygous54745071
6136521562136521563CG32GENIChomozygous54745073
6136507074136507075AG10GENIChomozygous56009871
6136507076136507082ACACAC------10GENIChomozygous56009873