| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33083895-33084003 | Rare:11 | ||||
| chr3:33316482-33316690 | Common:2; Rare:36 | ||||
| chr3:33339218-33339304 | Rare:13 | ||||
| chr3:33400962-33401121 | Rare:41 | ||||
| chr3:33857524-33857634 | Common:1; Rare:19 | ||||
| chr3:33861446-33861553 | Common:1; Rare:23 | ||||
| chr3:37048473-37048579 | Rare:32; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr3:37091468-37091749 | Common:1; Rare:75 | ||||
| chr3:37299004-37299368 | Rare:93 | ||||
| chr3:38498600-38498853 | Common:1; Rare:32 | ||||
| chr3:39079526-39079714 | Common:1; Rare:32 | ||||
| chr3:40453133-40453417 | Common:6; Rare:68 | ||||
| chr3:41203122-41203197 | Rare:11 | ||||
| chr3:43874846-43874971 | Rare:13 | ||||
| chr3:43994908-43995034 | Rare:29 |