Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:119057070-119057489 | Common:3; Rare:161 | ||||
chr11:119067624-119067822 | Common:3; Rare:65 | ||||
chr11:119087769-119087987 | Rare:33 | ||||
chr11:119121269-119121626 | Common:1; Rare:84 | ||||
chr11:119206175-119206331 | Common:5; Rare:74; Clinvar:6; Clinvar (benign):4 | ||||
chr11:119334286-119334527 | Rare:66 | ||||
chr11:120210804-120211032 | Rare:62 | ||||
chr11:121292623-121292804 | Rare:62; Clinvar:3 | ||||
chr11:121590224-121590372 | Common:1; Rare:23 | ||||
chr11:124673700-124673974 | Common:5; Rare:81 | ||||
chr11:124876779-124876907 | Common:1; Rare:29 | ||||
chr11:124897842-124897967 | Common:2; Rare:32 | ||||
chr11:124953976-124954117 | Common:3; Rare:37 | ||||
chr11:125592466-125592904 | Common:6; Rare:149 | ||||
chr11:125625628-125625997 | Common:3; Rare:126 |