| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10454893-10455414 | Common:7; Rare:98; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10455918-10456056 | Rare:18 | ||||
| chr11:10456305-10456371 | Rare:13 | ||||
| chr11:10508564-10508707 | Common:1; Rare:33 | ||||
| chr11:10509042-10509332 | Common:4; Rare:71 | ||||
| chr11:10541102-10541321 | Common:1; Rare:80 | ||||
| chr11:10594466-10594766 | Common:3; Rare:55 | ||||
| chr11:10750852-10751046 | Common:3; Rare:57 | ||||
| chr11:10751184-10751384 | Rare:65 | ||||
| chr11:10798967-10799363 | Common:3; Rare:133 | ||||
| chr11:10799374-10799797 | Common:4; Rare:122 | ||||
| chr11:10800059-10800668 | Common:1; Rare:166 | ||||
| chr11:10801531-10801777 | Rare:81 | ||||
| chr11:10806845-10806921 | Rare:33 | ||||
| chr11:10808484-10809006 | Common:1; Rare:191 |