| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:86432994-86433034 | Common:1; Rare:14 | ||||
| chr11:86454291-86454450 | Rare:20 | ||||
| chr11:86503574-86503732 | Common:1; Rare:24 | ||||
| chr11:86938420-86938522 | Common:1; Rare:18 | ||||
| chr11:86955998-86956132 | Common:1; Rare:39 | ||||
| chr11:87832414-87832577 | Rare:31 | ||||
| chr11:88819885-88820032 | Common:2; Rare:24 | ||||
| chr11:90130881-90130992 | Rare:17 | ||||
| chr11:90167571-90167974 | Common:6; Rare:105 | ||||
| chr11:91794222-91794429 | Common:2; Rare:47 | ||||
| chr11:92915605-92915762 | Common:2; Rare:38 | ||||
| chr11:93524844-93524985 | Common:1; Rare:15 | ||||
| chr11:94492841-94492952 | Rare:19; Clinvar (benign):1 | ||||
| chr11:94512371-94512513 | Common:1; Rare:35 | ||||
| chr11:94730839-94731029 | Rare:33 |