| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792589-9792651 | Rare:19 | ||||
| chr3:9792676-9793136 | Common:3; Rare:161 | ||||
| chr3:9843856-9844140 | Common:4; Rare:127 | ||||
| chr3:9890457-9890722 | Common:3; Rare:111 | ||||
| chr3:9933514-9933884 | Common:2; Rare:151; Clinvar:3 | ||||
| chr3:9933987-9934080 | Rare:23 | ||||
| chr3:10026283-10026486 | Common:1; Rare:65 | ||||
| chr3:10115518-10115819 | Common:4; Rare:92 | ||||
| chr3:10141678-10141875 | Common:1; Rare:91; Clinvar:16; Clinvar (benign):19 | ||||
| chr3:10248220-10248534 | Common:5; Rare:97 | ||||
| chr3:11643591-11643662 | Rare:12 | ||||
| chr3:11643701-11644016 | Common:2; Rare:77 | ||||
| chr3:11719453-11719542 | Rare:27 | ||||
| chr3:12004152-12004349 | Common:4; Rare:44 | ||||
| chr3:12158844-12159045 | Rare:68 |