| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64318067-64318346 | Common:1; Rare:129 | ||||
| chr11:64778447-64778599 | Rare:85 | ||||
| chr11:64810489-64810821 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:64917197-64917558 | Common:3; Rare:84 | ||||
| chr11:65014081-65014228 | Rare:31 | ||||
| chr11:65084028-65084272 | Common:1; Rare:72 | ||||
| chr11:65117659-65117979 | Common:5; Rare:111 | ||||
| chr11:65181860-65181987 | Rare:25 | ||||
| chr11:65333780-65333881 | Common:1; Rare:57 | ||||
| chr11:65386514-65386657 | Rare:47 | ||||
| chr11:65570378-65570500 | Rare:55 | ||||
| chr11:65638035-65638113 | Common:1; Rare:37 | ||||
| chr11:65662877-65662994 | Common:1; Rare:36 | ||||
| chr11:65833750-65833976 | Rare:50 | ||||
| chr11:65860182-65860441 | Common:1; Rare:86 |