| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17077490-17077950 | Common:6; Rare:306 | ||||
| chr11:17207908-17208153 | Common:4; Rare:167 | ||||
| chr11:17208270-17208610 | Rare:134 | ||||
| chr11:17276456-17276823 | Common:9; Rare:207; Clinvar:7; Clinvar (pathogenic):2 | ||||
| chr11:17351620-17352299 | Common:5; Rare:235 | ||||
| chr11:17544349-17544499 | Common:5; Rare:65; Clinvar:4 | ||||
| chr11:18012889-18013266 | Common:6; Rare:126 | ||||
| chr11:18322075-18322330 | Common:7; Rare:178; Clinvar:4; Clinvar (benign):4 | ||||
| chr11:18322455-18322640 | Common:4; Rare:134 | ||||
| chr11:18394357-18394644 | Common:2; Rare:188; Clinvar (benign):2 | ||||
| chr11:18526825-18527014 | Common:2; Rare:178 | ||||
| chr11:18588654-18588905 | Common:4; Rare:179 | ||||
| chr11:18634313-18634605 | Common:4; Rare:181 | ||||
| chr11:18634710-18634930 | Common:3; Rare:54 | ||||
| chr11:19240764-19241301 | Rare:221 |