| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:106077335-106077711 | Common:2; Rare:114 | ||||
| chr11:108009273-108009349 | Rare:38 | ||||
| chr11:108222594-108223115 | Common:1; Rare:167; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:108929304-108929673 | Common:1; Rare:63 | ||||
| chr11:111766342-111766433 | Common:1; Rare:54 | ||||
| chr11:111879158-111879471 | Rare:88 | ||||
| chr11:111879474-111879539 | Rare:22 | ||||
| chr11:111911957-111912147 | Common:3; Rare:37 | ||||
| chr11:111912712-111912847 | Rare:22 | ||||
| chr11:111913128-111913294 | Rare:46 | ||||
| chr11:112073995-112074383 | Common:1; Rare:82 | ||||
| chr11:112086719-112086909 | Rare:79; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:112226315-112226452 | Rare:61 | ||||
| chr11:113314453-113314595 | Rare:50 | ||||
| chr11:113875497-113875781 | Common:4; Rare:106 |