chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42973099829730999GA9GENICheterozygous811669957
42973205829732059AT8GENIChomozygous811669958
42973519329735194AG79GENICheterozygous811669959
42973530829735309AG81GENICheterozygous811669960
42974714329747144CT20GENIChomozygous811669961
42974756029747561AT26GENIChomozygous811669962
42974774829747749TG21GENIChomozygous811669963
42974784529747846GA23GENIChomozygous811669964
42974840229748403AT15GENIChomozygous811669965
42974867429748675AG9GENIChomozygous811669966
42974907729749078GT4GENIChomozygous811669967
42976430729764308AT11GENIChomozygous811669968
42976446229764463GA20GENIChomozygous811669969
42976452029764521CT20GENIChomozygous811669970
42976470129764702CA9GENIChomozygous811669971
42976488529764886AG11GENIChomozygous811669972
42976493929764940CT10GENIChomozygous811669973
42976497329764974CA11GENIChomozygous811669974
42976729829767299AG23GENIChomozygous811669975
42976741029767411AG16GENIChomozygous811669976
42976743729767438GT24GENIChomozygous811669977
42976749729767498CA15GENIChomozygous811669978