| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17207895-17208072 | Common:2; Rare:70 | ||||
| chr11:17310992-17311260 | Rare:52 | ||||
| chr11:18322086-18322306 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322457-18322613 | Common:2; Rare:64 | ||||
| chr11:18394540-18394628 | Rare:36 | ||||
| chr11:18588649-18588809 | Rare:64 | ||||
| chr11:20387417-20387738 | Common:7; Rare:103 | ||||
| chr11:27506718-27506864 | Common:1; Rare:68 | ||||
| chr11:27699075-27699213 | Common:1; Rare:24 | ||||
| chr11:27700464-27700521 | Common:1; Rare:9 | ||||
| chr11:28108073-28108430 | Common:1; Rare:106 | ||||
| chr11:30322879-30323162 | Common:2; Rare:81 | ||||
| chr11:31369735-31369915 | Rare:54 | ||||
| chr11:31509596-31509782 | Common:1; Rare:59 | ||||
| chr11:33015784-33015901 | Rare:41 |