chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45639289156392892AG38GENIChomozygous56905940
45639324256393243CCA11GENICheterozygous58464547
45639324256393243CCAA11GENICheterozygous58334992
45639416856394169AT21GENIChomozygous56905941
45639434456394345T-21GENIChomozygous56905942
45639453956394540TC41GENIChomozygous56905943
45639519856395200GT--20GENIChomozygous56905945
45639521156395219CGCGCACA--------21GENICpossibly homozygous58334993
45639680556396806GA29GENIChomozygous56905948
45640123456401235GA26GENIChomozygous56905949
45640392656403927GGT8GENIChomozygous56905950
45640506056405061TA27GENIChomozygous56905951
45640523356405235TT--20GENICheterozygous56905952
45640523456405235T-20GENICheterozygous56905953
45640658156406582GC30GENIChomozygous56905954
45640670956406710GA42GENIChomozygous56905955
45640678956406790GC48GENIChomozygous56905956
45640907856409079C-2GENIChomozygous58334994
45641623556416236CCTG47GENIChomozygous56905961
45641172556411726AG31GENIChomozygous56905959
45641251956412520GT22GENIChomozygous56905960
45641534156415342GGCGCACACACACACA9GENICheterozygous58334995
45641595256415978CAAGTTATTTTGAGACAAGTTCTCAT--------------------------32GENIChomozygous58334996
45641723556417236AC55GENIChomozygous56905962
45641744456417445AAGG5GENIChomozygous58406668
45641783356417834AAGTGT13GENICpossibly homozygous56905965
45641993156419932GA43GENIChomozygous56905966