| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322469-18322721 | Common:2; Rare:92 | ||||
| chr11:18396057-18396395 | Common:1; Rare:118 | ||||
| chr11:18526782-18526977 | Common:1; Rare:85 | ||||
| chr11:18588661-18588942 | Common:4; Rare:90 | ||||
| chr11:18634182-18634497 | Common:2; Rare:114 | ||||
| chr11:18698582-18698758 | Common:4; Rare:46 | ||||
| chr11:18791772-18792002 | Common:1; Rare:81 | ||||
| chr11:19241595-19241868 | Common:1; Rare:80 | ||||
| chr11:20363682-20363753 | Rare:17 | ||||
| chr11:20387417-20387771 | Common:7; Rare:115 | ||||
| chr11:20669456-20669665 | Common:3; Rare:89 | ||||
| chr11:22192994-22193116 | Rare:28 | ||||
| chr11:22625499-22625613 | Rare:57; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625798-22626016 | Common:3; Rare:74; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:26994061-26994168 | Common:1; Rare:16 |