| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14643627-14643810 | Common:1; Rare:70 | ||||
| chr11:14891627-14891811 | Rare:55 | ||||
| chr11:16738426-16738844 | Common:3; Rare:104 | ||||
| chr11:17014025-17014332 | Common:1; Rare:119 | ||||
| chr11:17077607-17077854 | Common:2; Rare:103 | ||||
| chr11:17207916-17208102 | Common:2; Rare:69 | ||||
| chr11:17276541-17276828 | Common:5; Rare:82; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:17389321-17389481 | Common:2; Rare:31 | ||||
| chr11:18012909-18013254 | Common:6; Rare:114 | ||||
| chr11:18322075-18322300 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322467-18322645 | Common:2; Rare:73 | ||||
| chr11:18394331-18394645 | Common:1; Rare:124; Clinvar (benign):1 | ||||
| chr11:18396160-18396410 | Common:1; Rare:95 | ||||
| chr11:18526812-18527063 | Common:2; Rare:114 | ||||
| chr11:18588667-18588933 | Common:3; Rare:86 |