| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61332949-61333526 | Common:3; Rare:463 | ||||
| chr11:61361760-61362463 | Common:9; Rare:375; Clinvar:21; Clinvar (benign):2 | ||||
| chr11:61392040-61392462 | Common:3; Rare:113; Clinvar:3 | ||||
| chr11:61392433-61393010 | Common:7; Rare:271; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr11:61429430-61429607 | Common:2; Rare:55 | ||||
| chr11:61429560-61429830 | Common:2; Rare:142 | ||||
| chr11:61429852-61430252 | Common:5; Rare:443; Clinvar:9; Clinvar (benign):23 | ||||
| chr11:61488520-61489010 | Common:12; Rare:162 | ||||
| chr11:61489002-61489286 | Common:10; Rare:136 | ||||
| chr11:61508836-61509764 | Common:4; Rare:456 | ||||
| chr11:61580958-61581301 | Common:6; Rare:216 | ||||
| chr11:61581466-61581866 | Rare:135 | ||||
| chr11:61680245-61680473 | Common:3; Rare:193 | ||||
| chr11:61791827-61792234 | Common:1; Rare:96 | ||||
| chr11:61792504-61793035 | Common:18; Rare:408 |