| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111794128-111794342 | Common:1; Rare:33 | ||||
| chr11:114061938-114062211 | Common:6; Rare:56 | ||||
| chr11:114153257-114153590 | Common:1; Rare:56 | ||||
| chr11:114176341-114176531 | Rare:29 | ||||
| chr11:114294994-114295272 | Rare:49 | ||||
| chr11:114308519-114308839 | Common:1; Rare:53 | ||||
| chr11:116813997-116814217 | Common:3; Rare:39 | ||||
| chr11:116832418-116832540 | Common:1; Rare:17 | ||||
| chr11:116832600-116832938 | Common:3; Rare:101; Clinvar (pathogenic):2 | ||||
| chr11:116836341-116836524 | Common:1; Rare:49 | ||||
| chr11:118791680-118791756 | Common:1; Rare:19 | ||||
| chr11:120212701-120212828 | Rare:26 | ||||
| chr11:120337734-120337847 | Common:1; Rare:20 | ||||
| chr11:126304269-126304326 | Rare:32 | ||||
| chr11:126655860-126656054 | Rare:36 |