| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18394401-18394626 | Common:1; Rare:92; Clinvar (benign):1 | ||||
| chr11:18526812-18527001 | Common:1; Rare:86 | ||||
| chr11:18588679-18588815 | Rare:43 | ||||
| chr11:18634336-18634588 | Common:2; Rare:81 | ||||
| chr11:18791731-18791956 | Common:1; Rare:80 | ||||
| chr11:20387434-20387749 | Common:7; Rare:105 | ||||
| chr11:22625518-22625618 | Rare:53; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626004 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27506701-27506868 | Common:1; Rare:79 | ||||
| chr11:28108115-28108421 | Common:1; Rare:94 | ||||
| chr11:30322944-30323180 | Common:2; Rare:68 | ||||
| chr11:31369724-31369912 | Rare:56 | ||||
| chr11:31509555-31509946 | Common:1; Rare:145 | ||||
| chr11:31811217-31811469 | Rare:40; Clinvar:2 | ||||
| chr11:32583622-32583914 | Rare:107 |