| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:416990-417262 | Common:2; Rare:104 | ||||
| chr11:417284-417609 | Rare:174 | ||||
| chr11:441910-442073 | Common:2; Rare:91 | ||||
| chr11:448030-448366 | Common:8; Rare:250 | ||||
| chr11:450042-450583 | Common:4; Rare:289 | ||||
| chr11:506250-506504 | Common:4; Rare:82 | ||||
| chr11:506632-507061 | Common:9; Rare:333 | ||||
| chr11:507086-507598 | Common:12; Rare:444 | ||||
| chr11:534504-534854 | Common:2; Rare:132 | ||||
| chr11:534887-535390 | Common:7; Rare:211 | ||||
| chr11:535411-535860 | Common:22; Rare:459; Clinvar (benign):2 | ||||
| chr11:537213-537580 | Common:17; Rare:289 | ||||
| chr11:560089-560505 | Common:6; Rare:234 | ||||
| chr11:560595-561110 | Common:27; Rare:574 | ||||
| chr11:561558-561900 | Common:1; Rare:204 |