| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94768064-94768446 | Common:3; Rare:101 | ||||
| chr11:94973496-94973865 | Rare:103 | ||||
| chr11:95067448-95067899 | Common:3; Rare:183 | ||||
| chr11:95089712-95090035 | Common:3; Rare:124 | ||||
| chr11:95231406-95231620 | Common:2; Rare:59 | ||||
| chr11:95231950-95232069 | Rare:24 | ||||
| chr11:95232226-95232431 | Rare:40 | ||||
| chr11:95232434-95232491 | Rare:10 | ||||
| chr11:95789465-95790014 | Common:5; Rare:234 | ||||
| chr11:95790285-95790686 | Common:3; Rare:154 | ||||
| chr11:95923789-95924164 | Common:2; Rare:157; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389846-96390083 | Common:2; Rare:97 | ||||
| chr11:99020623-99021082 | Rare:134 | ||||
| chr11:101914752-101915330 | Common:8; Rare:151 | ||||
| chr11:102347101-102347317 | Common:2; Rare:69 |