| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112086719-112086919 | Rare:84; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:112226314-112226446 | Rare:61 | ||||
| chr11:112961316-112961638 | Common:4; Rare:161 | ||||
| chr11:113314448-113314616 | Rare:61 | ||||
| chr11:113875475-113875771 | Common:4; Rare:106 | ||||
| chr11:114059428-114059727 | Rare:64 | ||||
| chr11:114400444-114400755 | Common:2; Rare:124 | ||||
| chr11:116772924-116773066 | Rare:59 | ||||
| chr11:117179020-117179180 | Rare:30 | ||||
| chr11:117199017-117199424 | Common:6; Rare:130 | ||||
| chr11:117232520-117232760 | Common:2; Rare:83 | ||||
| chr11:117316257-117316432 | Common:1; Rare:38 | ||||
| chr11:117824640-117824942 | Common:2; Rare:76; Clinvar (benign):2 | ||||
| chr11:117986293-117986464 | Common:3; Rare:68; Clinvar:2 | ||||
| chr11:118252089-118252211 | Rare:49 |