| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9792355-9792580 | Rare:66 | ||||
| chr3:9792685-9793124 | Common:3; Rare:155 | ||||
| chr3:9843968-9844155 | Common:2; Rare:69 | ||||
| chr3:9917017-9917186 | Common:1; Rare:32 | ||||
| chr3:9933517-9933910 | Common:3; Rare:156; Clinvar:3 | ||||
| chr3:9933965-9934083 | Rare:27 | ||||
| chr3:10026254-10026489 | Common:1; Rare:69 | ||||
| chr3:10115520-10115734 | Common:3; Rare:79 | ||||
| chr3:11272233-11272427 | Common:1; Rare:43 | ||||
| chr3:11643731-11644184 | Common:4; Rare:106 | ||||
| chr3:11719432-11719595 | Rare:51 | ||||
| chr3:11846843-11847027 | Common:1; Rare:52 | ||||
| chr3:12004231-12004356 | Common:1; Rare:35 | ||||
| chr3:12664071-12664315 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12796475-12796718 | Common:5; Rare:65 |