| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14643627-14643748 | Common:1; Rare:57 | ||||
| chr11:14892199-14892282 | Rare:30 | ||||
| chr11:16738466-16738839 | Common:3; Rare:88 | ||||
| chr11:17077608-17077934 | Common:2; Rare:135 | ||||
| chr11:17207916-17208085 | Common:2; Rare:63 | ||||
| chr11:17351637-17351806 | Rare:36 | ||||
| chr11:17351824-17352020 | Common:2; Rare:42 | ||||
| chr11:18322131-18322631 | Common:8; Rare:177; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18394422-18394630 | Common:1; Rare:82; Clinvar (benign):1 | ||||
| chr11:18526841-18526972 | Rare:65 | ||||
| chr11:18588667-18588873 | Common:2; Rare:71 | ||||
| chr11:22625808-22626002 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26994049-26994174 | Common:1; Rare:18 | ||||
| chr11:27506721-27506875 | Common:1; Rare:72 | ||||
| chr11:28108134-28108421 | Common:1; Rare:86 |