| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47214769-47215019 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:47216177-47216577 | Common:1; Rare:158; Clinvar:3 | ||||
| chr11:47248778-47249198 | Rare:119 | ||||
| chr11:47268406-47268806 | Common:1; Rare:153; Clinvar (pathogenic):2 | ||||
| chr11:47268962-47269390 | Common:1; Rare:81 | ||||
| chr11:47269501-47269717 | Common:1; Rare:72 | ||||
| chr11:47269959-47270188 | Common:1; Rare:77 | ||||
| chr11:47408094-47408611 | Common:2; Rare:149 | ||||
| chr11:47426370-47426670 | Common:1; Rare:75 | ||||
| chr11:47552492-47552892 | Common:5; Rare:219 | ||||
| chr11:47553121-47553394 | Common:1; Rare:82 | ||||
| chr11:47565390-47565990 | Common:5; Rare:163 | ||||
| chr11:47578561-47578867 | Rare:72 | ||||
| chr11:47578946-47579094 | Rare:76; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47594280-47594660 | Common:3; Rare:101 |