| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:151384748-151385039 | Common:1; Rare:59 | ||||
| chr3:152268439-152269347 | Common:3; Rare:299; Clinvar (benign):1 | ||||
| chr3:152269508-152269772 | Common:2; Rare:75 | ||||
| chr3:152269845-152270060 | Common:4; Rare:55 | ||||
| chr3:152298942-152299207 | Common:1; Rare:53 | ||||
| chr3:154121266-154121446 | Common:2; Rare:77 | ||||
| chr3:154324314-154324573 | Rare:102 | ||||
| chr3:155854355-155854765 | Rare:111 | ||||
| chr3:156291740-156291888 | Common:3; Rare:45 | ||||
| chr3:156674364-156674647 | Common:3; Rare:82 | ||||
| chr3:157159843-157160285 | Common:1; Rare:166 | ||||
| chr3:158571061-158571255 | Common:1; Rare:61 | ||||
| chr3:158672540-158672805 | Common:4; Rare:69 | ||||
| chr3:158732150-158732488 | Common:10; Rare:118 | ||||
| chr3:158801984-158802147 | Common:2; Rare:78 |