| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179451364-179451628 | Common:1; Rare:92 | ||||
| chr3:179562621-179562993 | Rare:127 | ||||
| chr3:179604605-179604936 | Common:3; Rare:131 | ||||
| chr3:179652895-179653200 | Common:2; Rare:88 | ||||
| chr3:180602094-180602348 | Common:1; Rare:89 | ||||
| chr3:180912393-180912722 | Common:2; Rare:114 | ||||
| chr3:180989572-180989790 | Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:182793334-182793638 | Common:3; Rare:82 | ||||
| chr3:182980490-182980875 | Common:3; Rare:131 | ||||
| chr3:183099443-183099774 | Common:2; Rare:101; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183428503-183428697 | Common:1; Rare:59 | ||||
| chr3:183635514-183635707 | Common:2; Rare:61 | ||||
| chr3:183697652-183697959 | Common:2; Rare:122 | ||||
| chr3:183884828-183884957 | Rare:55 | ||||
| chr3:184017851-184018109 | Common:2; Rare:82 |