| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68312528-68312720 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr11:68313006-68313497 | Common:2; Rare:115 | ||||
| chr11:68460175-68460324 | Common:2; Rare:75 | ||||
| chr11:68460513-68460844 | Common:3; Rare:111 | ||||
| chr11:68460945-68461005 | Rare:24 | ||||
| chr11:68751380-68751728 | Common:1; Rare:72 | ||||
| chr11:68839048-68839505 | Common:2; Rare:93 | ||||
| chr11:68841817-68841925 | Rare:36 | ||||
| chr11:68903772-68904124 | Common:7; Rare:148; Clinvar:6; Clinvar (benign):8 | ||||
| chr11:69013473-69013869 | Common:3; Rare:85 | ||||
| chr11:69048711-69049026 | Common:6; Rare:116 | ||||
| chr11:69293953-69294229 | Common:3; Rare:39 | ||||
| chr11:69295304-69295410 | Rare:44 | ||||
| chr11:69640739-69641292 | Common:1; Rare:127 | ||||
| chr11:69641441-69641469 | Rare:7 |