| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14358425-14358573 | Rare:36 | ||||
| chr11:14358766-14358947 | Rare:36 | ||||
| chr11:14359004-14359231 | Rare:74 | ||||
| chr11:14499359-14499641 | Common:1; Rare:66 | ||||
| chr11:14499701-14499935 | Common:2; Rare:81 | ||||
| chr11:14517725-14517762 | Rare:13 | ||||
| chr11:16607730-16607922 | Common:1; Rare:26 | ||||
| chr11:16738558-16738873 | Common:2; Rare:82 | ||||
| chr11:17077616-17077850 | Common:2; Rare:96 | ||||
| chr11:17207854-17207903 | Rare:9 | ||||
| chr11:17207905-17208082 | Common:2; Rare:70 | ||||
| chr11:17310922-17311240 | Rare:67 | ||||
| chr11:18105910-18106309 | Common:5; Rare:134 | ||||
| chr11:18322075-18322317 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322437-18322723 | Common:2; Rare:100 |