| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14891627-14891832 | Rare:60 | ||||
| chr11:16607730-16607988 | Common:1; Rare:38 | ||||
| chr11:16738466-16738854 | Common:3; Rare:92 | ||||
| chr11:17077595-17077857 | Common:2; Rare:109 | ||||
| chr11:17207889-17208111 | Common:2; Rare:85 | ||||
| chr11:17276566-17276828 | Common:4; Rare:68; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17351659-17352022 | Common:2; Rare:72 | ||||
| chr11:18012903-18013288 | Common:6; Rare:130 | ||||
| chr11:18106050-18106308 | Common:2; Rare:71 | ||||
| chr11:18322084-18322616 | Common:8; Rare:192; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18394393-18394612 | Common:1; Rare:88; Clinvar (benign):1 | ||||
| chr11:18526851-18526977 | Rare:60 | ||||
| chr11:18588672-18588905 | Common:2; Rare:78 | ||||
| chr11:18634300-18634588 | Common:3; Rare:96 | ||||
| chr11:18634785-18634904 | Common:1; Rare:29 |