chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77540968275409683A-2INTERGENICheterozygous55130670
77540969875409699GA7INTERGENIChomozygous54658373
77541046875410469AG10INTERGENIChomozygous53979066
77541116075411161CT13INTERGENIChomozygous53979068
77541192875411929AATCTCTCC4INTERGENIChomozygous53979070
77541208275412083CT22INTERGENIChomozygous53979072
77541238375412384AG17INTERGENIChomozygous53979074
77541295275412953AG16INTERGENICheterozygous53979076
77541356075413561C-22INTERGENICheterozygous54658375
77541402275414023CT21INTERGENICpossibly homozygous53979078
77541461075414611GC31INTERGENICpossibly homozygous53979082
77541493975414940AAGAG6INTERGENICheterozygous53979084
77541512175415122TTA1INTERGENIChomozygous53979086
77541556075415561TC21INTERGENICpossibly homozygous53979090
77541670575416821AGTGTATGTGTTCATGTGTGTGTCTGTATGTGCATATGCTTATGTGTGTGTGAGTGTATGTGTGCATGTGTGTGTATGTGTTTATGTGTGTGTGTGTATGTGTATGTGTGAGTGTA--------------------------------------------------------------------------------------------------------------------14INTERGENIChomozygous55130672
77541690975416911TG--2INTERGENIChomozygous53979106
77541707175417072TC17INTERGENICheterozygous53979108
77541710775417108AAGTGTGTGTGTGTGTGTGTGTGT2INTERGENIChomozygous55130674
77541780875417809AG6INTERGENIChomozygous53979112
77541792275417923CT24INTERGENICpossibly homozygous53979114
77541821375418214TC14INTERGENIChomozygous53979120
77541843275418433AG27INTERGENIChomozygous53979122
77541895775418958GT20INTERGENICpossibly homozygous53979128
77541924575419246AG9INTERGENIChomozygous53979130
77541976975419770GT24INTERGENICpossibly homozygous53979132
77541992175419922CT14INTERGENICpossibly homozygous53979134
77542072475420725GA5INTERGENIChomozygous53979138
77542073975420740TC11INTERGENIChomozygous53979140
77542085275420853TG17INTERGENICpossibly homozygous53979142
77542124275421243GA14INTERGENIChomozygous53979144