| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14358451-14358577 | Rare:28 | ||||
| chr11:14358785-14359077 | Rare:72 | ||||
| chr11:14359113-14359210 | Rare:34 | ||||
| chr11:14520067-14520566 | Common:1; Rare:144 | ||||
| chr11:14643620-14643887 | Common:1; Rare:97 | ||||
| chr11:16738450-16738956 | Common:3; Rare:126 | ||||
| chr11:17013337-17013496 | Rare:57 | ||||
| chr11:17013850-17014327 | Common:7; Rare:188 | ||||
| chr11:17077575-17077899 | Common:3; Rare:144 | ||||
| chr11:17207858-17208099 | Common:2; Rare:85 | ||||
| chr11:17208359-17208559 | Rare:34 | ||||
| chr11:17351600-17351821 | Common:1; Rare:49 | ||||
| chr11:18105906-18106311 | Common:5; Rare:137 | ||||
| chr11:18322071-18322314 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322457-18322687 | Common:2; Rare:84 |