| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33798372-33798647 | Common:2; Rare:75 | ||||
| chr3:36993124-36993523 | Common:2; Rare:120; Clinvar:21; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr3:39051917-39052052 | Common:1; Rare:46 | ||||
| chr3:39107597-39107680 | Common:2; Rare:26 | ||||
| chr3:39406600-39406761 | Common:2; Rare:69 | ||||
| chr3:40309515-40309803 | Common:8; Rare:103 | ||||
| chr3:42160182-42160258 | Common:1; Rare:11 | ||||
| chr3:42581932-42582106 | Common:2; Rare:50 | ||||
| chr3:42600377-42600777 | Common:2; Rare:152 | ||||
| chr3:42804434-42804627 | Common:2; Rare:57 | ||||
| chr3:43286449-43286648 | Common:2; Rare:89 | ||||
| chr3:44477655-44477752 | Common:1; Rare:15 | ||||
| chr3:44761583-44761794 | Common:3; Rare:77 | ||||
| chr3:44976126-44976272 | Common:2; Rare:63 | ||||
| chr3:45689154-45689459 | Common:2; Rare:104 |