| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111541718-111541781 | Rare:13 | ||||
| chr11:111879154-111879549 | Common:1; Rare:119 | ||||
| chr11:111912057-111912123 | Common:2; Rare:13 | ||||
| chr11:112025284-112025480 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112073995-112074361 | Common:1; Rare:76 | ||||
| chr11:112074730-112074864 | Rare:18 | ||||
| chr11:112086716-112086881 | Rare:67 | ||||
| chr11:113314450-113314608 | Rare:57 | ||||
| chr11:114400401-114400753 | Common:2; Rare:135 | ||||
| chr11:117199020-117199466 | Common:6; Rare:133 | ||||
| chr11:117200008-117200213 | Common:6; Rare:42 | ||||
| chr11:117202960-117203448 | Common:5; Rare:171 | ||||
| chr11:117232504-117232736 | Common:2; Rare:74 | ||||
| chr11:117281344-117281476 | Rare:26 | ||||
| chr11:117316211-117316408 | Common:1; Rare:47 |