| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118997977-118998199 | Common:4; Rare:69 | ||||
| chr11:119018257-119018479 | Common:7; Rare:87 | ||||
| chr11:119018567-119018819 | Common:5; Rare:93 | ||||
| chr11:119057068-119057438 | Common:3; Rare:142 | ||||
| chr11:119067624-119067824 | Common:3; Rare:65 | ||||
| chr11:119095363-119095765 | Common:3; Rare:135 | ||||
| chr11:119101789-119102189 | Rare:101; Clinvar:4 | ||||
| chr11:119121307-119121631 | Common:1; Rare:70 | ||||
| chr11:119168074-119168433 | Common:2; Rare:76; Clinvar:2 | ||||
| chr11:119168567-119168788 | Rare:38; Clinvar:1 | ||||
| chr11:119206175-119206383 | Common:5; Rare:96; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119334283-119334556 | Rare:73 | ||||
| chr11:119381597-119381826 | Common:1; Rare:52 | ||||
| chr11:119729421-119729587 | Rare:41 | ||||
| chr11:120122952-120123223 | Common:2; Rare:96 |