| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:8682628-8682820 | Common:2; Rare:85 | ||||
| chr11:8717935-8718169 | Common:7; Rare:58 | ||||
| chr11:8964364-8964564 | Common:4; Rare:65 | ||||
| chr11:8964932-8965122 | Common:2; Rare:46 | ||||
| chr11:9460697-9461003 | Common:3; Rare:84 | ||||
| chr11:9664010-9664217 | Common:4; Rare:78 | ||||
| chr11:10304818-10305102 | Common:1; Rare:66 | ||||
| chr11:10750697-10751019 | Common:4; Rare:85 | ||||
| chr11:10858023-10858269 | Common:2; Rare:78 | ||||
| chr11:12377472-12377650 | Rare:73 | ||||
| chr11:14520297-14520437 | Rare:51 | ||||
| chr11:16738466-16738707 | Common:3; Rare:52 | ||||
| chr11:17207906-17208082 | Common:2; Rare:69 | ||||
| chr11:17351693-17351806 | Rare:21 | ||||
| chr11:18322124-18322631 | Common:8; Rare:182; Clinvar:1; Clinvar (benign):2 |