| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:313701-314201 | Common:1; Rare:200 | ||||
| chr11:320821-321045 | Common:10; Rare:53 | ||||
| chr11:369110-369600 | Common:13; Rare:119 | ||||
| chr11:370133-370264 | Common:1; Rare:33 | ||||
| chr11:447990-448490 | Common:5; Rare:141 | ||||
| chr11:450137-450358 | Common:1; Rare:68 | ||||
| chr11:506670-507080 | Common:4; Rare:127 | ||||
| chr11:507175-507544 | Common:4; Rare:120 | ||||
| chr11:535429-535817 | Common:8; Rare:157; Clinvar (benign):1 | ||||
| chr11:560580-561010 | Common:6; Rare:193 | ||||
| chr11:576402-576503 | Rare:36 | ||||
| chr11:615944-616132 | Common:1; Rare:60 | ||||
| chr11:638539-639782 | Common:14; Rare:633 | ||||
| chr11:695003-695202 | Common:1; Rare:49 | ||||
| chr11:695637-695934 | Common:2; Rare:85 |