| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:11621952-11622214 | Common:3; Rare:103 | ||||
| chr11:11841941-11842083 | Common:1; Rare:39 | ||||
| chr11:12110367-12110674 | Rare:76 | ||||
| chr11:12377474-12377782 | Rare:108 | ||||
| chr11:12398007-12398285 | Common:4; Rare:43 | ||||
| chr11:12473768-12473983 | Rare:71 | ||||
| chr11:13463141-13463358 | Common:1; Rare:78 | ||||
| chr11:14520297-14520431 | Rare:49 | ||||
| chr11:14643588-14643830 | Common:2; Rare:93 | ||||
| chr11:16738466-16738853 | Common:3; Rare:91 | ||||
| chr11:17077565-17077868 | Common:3; Rare:132 | ||||
| chr11:17207908-17208104 | Common:2; Rare:75 | ||||
| chr11:18012896-18013248 | Common:6; Rare:118 | ||||
| chr11:18106045-18106308 | Common:2; Rare:75 | ||||
| chr11:18322124-18322321 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):2 |