chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45639289156392892AG16GENIChomozygous56905940
45639324256393243CCAA6GENIChomozygous58334992
45639416856394169AT19GENIChomozygous56905941
45639434456394345T-12GENICheterozygous56905942
45639453956394540TC30GENIChomozygous56905943
45639519856395200GT--2GENIChomozygous56905945
45639521156395219CGCGCACA--------4GENICheterozygous58334993
45639680556396806GA21GENIChomozygous56905948
45640123456401235GA23GENIChomozygous56905949
45640392656403927GGT5GENIChomozygous56905950
45640506056405061TA20GENIChomozygous56905951
45640523456405235T-4GENIChomozygous56905953
45640658156406582GC18GENIChomozygous56905954
45640670956406710GA32GENIChomozygous56905955
45640678956406790GC28GENIChomozygous56905956
45640907856409079C-1GENIChomozygous58334994
45641172556411726AG25GENIChomozygous56905959
45641251956412520GT32GENIChomozygous56905960
45641534156415342GGCGCACACACACACA5GENICheterozygous58334995
45641595256415978CAAGTTATTTTGAGACAAGTTCTCAT--------------------------15GENIChomozygous58334996
45641623556416236CCTG28GENIChomozygous56905961
45641723556417236AC23GENIChomozygous56905962
45641744456417445AAGG3GENIChomozygous58406668
45641783356417834AAGTGT6GENIChomozygous56905965
45641993156419932GA39GENICpossibly homozygous56905966