| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:161276473-161276554 | Common:1; Rare:15 | ||||
| chr3:169764853-169764911 | Rare:23; Clinvar:6; Clinvar (pathogenic):1 | ||||
| chr3:169764949-169765324 | Common:1; Rare:125; Clinvar:7; Clinvar (pathogenic):6 | ||||
| chr3:179401149-179401455 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:182895035-182895052 | Rare:4 | ||||
| chr3:183267796-183267839 | Rare:5 | ||||
| chr3:184322540-184322954 | Rare:117; Clinvar:1 | ||||
| chr3:185920408-185920503 | Common:1; Rare:27 | ||||
| chr3:187738742-187739057 | Common:3; Rare:66 | ||||
| chr3:187739114-187739202 | Common:1; Rare:17 | ||||
| chr3:187739213-187739287 | Common:1; Rare:6 | ||||
| chr3:187739326-187739418 | Common:3; Rare:13 | ||||
| chr3:187740952-187741184 | Common:2; Rare:39 | ||||
| chr3:187741387-187741697 | Rare:58 | ||||
| chr3:187741967-187742250 | Common:4; Rare:53 |