| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65438544-65438666 | Common:1; Rare:25 | ||||
| chr11:65440169-65440418 | Rare:38 | ||||
| chr11:65443273-65443590 | Common:2; Rare:57 | ||||
| chr11:65455109-65455296 | Rare:85 | ||||
| chr11:65471460-65471697 | Rare:45 | ||||
| chr11:65472141-65472319 | Rare:26 | ||||
| chr11:65477434-65477646 | Common:2; Rare:69 | ||||
| chr11:65478831-65478987 | Rare:34 | ||||
| chr11:65489345-65489644 | Common:3; Rare:68 | ||||
| chr11:65493927-65494088 | Common:2; Rare:33 | ||||
| chr11:65497388-65497906 | Common:1; Rare:244 | ||||
| chr11:65498189-65498259 | Rare:41 | ||||
| chr11:65504139-65504257 | Common:1; Rare:55 | ||||
| chr11:65506664-65506816 | Common:2; Rare:55 | ||||
| chr11:65525958-65526277 | Common:1; Rare:107; Clinvar (pathogenic):2 |