| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118790894-118791316 | Rare:144 | ||||
| chr11:118997980-118998152 | Common:4; Rare:46 | ||||
| chr11:119018280-119018425 | Common:6; Rare:60 | ||||
| chr11:119018454-119018806 | Common:7; Rare:130 | ||||
| chr11:119057073-119057446 | Common:3; Rare:147 | ||||
| chr11:119067624-119067840 | Common:3; Rare:71 | ||||
| chr11:119084815-119084943 | Rare:41 | ||||
| chr11:119121306-119121626 | Common:1; Rare:69 | ||||
| chr11:119206180-119206369 | Common:5; Rare:85; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119311363-119311652 | Rare:100 | ||||
| chr11:119311806-119312166 | Common:1; Rare:124 | ||||
| chr11:119317024-119317284 | Rare:82 | ||||
| chr11:119334341-119334561 | Rare:59 | ||||
| chr11:122882845-122882922 | Rare:20 | ||||
| chr11:123062387-123062663 | Common:4; Rare:129 |