| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:171460073-171460379 | Common:2; Rare:69 | ||||
| chr3:171771347-171771513 | Common:1; Rare:32 | ||||
| chr3:172711058-172711176 | Rare:50 | ||||
| chr3:173397456-173397820 | Common:4; Rare:119 | ||||
| chr3:177196472-177196565 | Rare:28 | ||||
| chr3:177197129-177197391 | Rare:86 | ||||
| chr3:179148081-179148190 | Common:3; Rare:43 | ||||
| chr3:179347573-179347761 | Common:1; Rare:41 | ||||
| chr3:179451395-179451598 | Common:1; Rare:71 | ||||
| chr3:179604619-179604846 | Common:2; Rare:83 | ||||
| chr3:180601960-180602242 | Common:1; Rare:86 | ||||
| chr3:180989652-180989790 | Rare:60; Clinvar:1 | ||||
| chr3:181711736-181712047 | Rare:85 | ||||
| chr3:183099443-183099742 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183635510-183635699 | Common:2; Rare:61 |