| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:90223006-90223156 | Common:1; Rare:55 | ||||
| chr11:93732242-93732392 | Rare:53 | ||||
| chr11:93734622-93734774 | Common:1; Rare:39 | ||||
| chr11:93741330-93741702 | Common:8; Rare:146 | ||||
| chr11:93784196-93784369 | Common:3; Rare:53 | ||||
| chr11:94493757-94494053 | Common:5; Rare:87; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973502-94973739 | Rare:76 | ||||
| chr11:95089713-95089899 | Common:3; Rare:77 | ||||
| chr11:95789756-95789965 | Common:3; Rare:79 | ||||
| chr11:95790329-95790722 | Common:3; Rare:155; Clinvar:1 | ||||
| chr11:95923950-95924157 | Rare:91; Clinvar (benign):1 | ||||
| chr11:96389768-96390055 | Common:1; Rare:112 | ||||
| chr11:101915156-101915303 | Common:3; Rare:48 | ||||
| chr11:102317254-102317569 | Rare:65 | ||||
| chr11:102347115-102347376 | Common:2; Rare:87 |