| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:170222362-170222568 | Common:1; Rare:72 | ||||
| chr3:170418649-170418940 | Common:2; Rare:64 | ||||
| chr3:170870146-170870276 | Rare:77 | ||||
| chr3:172040384-172040608 | Common:1; Rare:54 | ||||
| chr3:172711051-172711160 | Rare:49 | ||||
| chr3:172750371-172750794 | Common:4; Rare:95 | ||||
| chr3:177196465-177196547 | Rare:19 | ||||
| chr3:179347573-179347788 | Common:1; Rare:52 | ||||
| chr3:179604614-179604915 | Common:2; Rare:120 | ||||
| chr3:180601902-180602242 | Common:1; Rare:93 | ||||
| chr3:180989610-180989790 | Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183099444-183099742 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183253056-183253353 | Common:3; Rare:81 | ||||
| chr3:183635507-183635677 | Common:1; Rare:52 | ||||
| chr3:183884822-183884969 | Rare:59 |