| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17013358-17013486 | Rare:47 | ||||
| chr11:17014264-17014664 | Common:10; Rare:288 | ||||
| chr11:17077600-17077945 | Common:2; Rare:141 | ||||
| chr11:17207898-17208180 | Common:2; Rare:110 | ||||
| chr11:17276527-17276777 | Common:4; Rare:72; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17389277-17389492 | Common:2; Rare:40 | ||||
| chr11:17476074-17476852 | Common:8; Rare:292; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr11:17516516-17516916 | Common:1; Rare:86 | ||||
| chr11:17734533-17734801 | Common:2; Rare:83 | ||||
| chr11:17735106-17735863 | Common:7; Rare:204 | ||||
| chr11:18012349-18012506 | Common:1; Rare:32 | ||||
| chr11:18012893-18013266 | Common:6; Rare:126 | ||||
| chr11:18322072-18322295 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322500-18322609 | Common:2; Rare:48 | ||||
| chr11:18396013-18396431 | Common:3; Rare:132 |