| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17077600-17077983 | Common:2; Rare:158 | ||||
| chr11:17078068-17078252 | Rare:50 | ||||
| chr11:17207619-17207724 | Rare:25 | ||||
| chr11:17207885-17208251 | Common:2; Rare:126 | ||||
| chr11:17208443-17208541 | Rare:23 | ||||
| chr11:17276255-17276317 | Rare:16 | ||||
| chr11:17276442-17276744 | Common:3; Rare:78; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18012866-18013435 | Common:6; Rare:176 | ||||
| chr11:18106016-18106310 | Common:2; Rare:96 | ||||
| chr11:18322037-18322368 | Common:6; Rare:118; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322420-18322652 | Common:2; Rare:88 | ||||
| chr11:18394324-18394799 | Common:3; Rare:168; Clinvar (benign):1 | ||||
| chr11:18395911-18396390 | Common:3; Rare:143 | ||||
| chr11:18526634-18526742 | Common:2; Rare:30 | ||||
| chr11:18526772-18527063 | Common:3; Rare:126 |