| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38138596-38138817 | Common:2; Rare:83; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:38165437-38165571 | Rare:46 | ||||
| chr3:39051944-39052052 | Common:1; Rare:40 | ||||
| chr3:39107553-39107725 | Common:3; Rare:54 | ||||
| chr3:39153539-39153714 | Common:3; Rare:58 | ||||
| chr3:39383289-39383443 | Common:2; Rare:26; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383547-39383666 | Rare:27; Clinvar:2 | ||||
| chr3:39809337-39809697 | Common:3; Rare:116 | ||||
| chr3:39810337-39810536 | Rare:47 | ||||
| chr3:40309446-40309819 | Common:9; Rare:127 | ||||
| chr3:40457223-40457368 | Common:2; Rare:69 | ||||
| chr3:40477059-40477184 | Common:1; Rare:32 | ||||
| chr3:40505945-40506110 | Rare:37 | ||||
| chr3:40524795-40525013 | Common:1; Rare:63 | ||||
| chr3:41238866-41239174 | Rare:87 |