| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:2138629-2138742 | Rare:25 | ||||
| chr11:2140910-2141066 | Rare:25 | ||||
| chr11:3840912-3841256 | Common:1; Rare:119 | ||||
| chr11:3856083-3856215 | Rare:45 | ||||
| chr11:4094594-4094877 | Common:2; Rare:78 | ||||
| chr11:5624903-5625023 | Rare:15 | ||||
| chr11:6390235-6390474 | Common:2; Rare:70 | ||||
| chr11:6481292-6481530 | Common:4; Rare:99 | ||||
| chr11:6603553-6603833 | Common:4; Rare:85; Clinvar (benign):3 | ||||
| chr11:6683261-6683652 | Common:6; Rare:148 | ||||
| chr11:7020323-7020462 | Rare:46 | ||||
| chr11:7513616-7513941 | Common:5; Rare:94 | ||||
| chr11:8682684-8682816 | Common:1; Rare:60 | ||||
| chr11:8910928-8911217 | Common:6; Rare:78 | ||||
| chr11:8964372-8964553 | Common:3; Rare:56 |