| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114354254-114354509 | Common:2; Rare:32 | ||||
| chr11:114401805-114401849 | Rare:6 | ||||
| chr11:114448071-114448215 | Rare:28 | ||||
| chr11:115503068-115503310 | Rare:70 | ||||
| chr11:115975641-115975680 | Rare:8 | ||||
| chr11:116193352-116193621 | Common:1; Rare:60 | ||||
| chr11:116193750-116193907 | Rare:43 | ||||
| chr11:116601897-116602014 | Common:1; Rare:23 | ||||
| chr11:116835907-116836183 | Rare:106; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr11:116865701-116866031 | Common:1; Rare:44 | ||||
| chr11:116972946-116972981 | Common:1; Rare:5 | ||||
| chr11:117018392-117018606 | Rare:29 | ||||
| chr11:117058863-117059066 | Common:2; Rare:46 | ||||
| chr11:117071428-117071729 | Common:1; Rare:60 | ||||
| chr11:117095716-117095999 | Common:1; Rare:41 |