| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94493789-94494027 | Common:3; Rare:68; Clinvar (benign):1 | ||||
| chr11:94973535-94973675 | Rare:40 | ||||
| chr11:95790410-95790557 | Rare:53 | ||||
| chr11:95923938-95924173 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:96389866-96390043 | Common:1; Rare:70 | ||||
| chr11:102347111-102347244 | Common:1; Rare:30 | ||||
| chr11:102452619-102452891 | Common:1; Rare:86 | ||||
| chr11:103092066-103092262 | Common:1; Rare:66 | ||||
| chr11:106077347-106077721 | Common:2; Rare:114 | ||||
| chr11:108222597-108222796 | Rare:68 | ||||
| chr11:111766363-111766417 | Rare:27 | ||||
| chr11:111878916-111879026 | Common:1; Rare:54 | ||||
| chr11:111879161-111879539 | Rare:110 | ||||
| chr11:112074011-112074349 | Common:1; Rare:68 | ||||
| chr11:112086721-112086905 | Rare:76; Clinvar:1 |