| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17207919-17208085 | Common:1; Rare:63 | ||||
| chr11:18322124-18322317 | Common:3; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322521-18322645 | Common:1; Rare:54 | ||||
| chr11:18394422-18394636 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr11:18396110-18396410 | Common:1; Rare:115 | ||||
| chr11:18526851-18526972 | Rare:59 | ||||
| chr11:18588672-18588860 | Common:2; Rare:63 | ||||
| chr11:18634292-18634588 | Common:3; Rare:101 | ||||
| chr11:20363656-20363735 | Common:1; Rare:18 | ||||
| chr11:22625808-22626011 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:24496704-24497015 | Common:2; Rare:90 | ||||
| chr11:26994089-26994168 | Common:1; Rare:12 | ||||
| chr11:27506721-27506877 | Common:1; Rare:72 | ||||
| chr11:28108110-28108414 | Common:1; Rare:92 | ||||
| chr11:30584164-30584356 | Common:3; Rare:24 |