| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38029605-38029770 | Common:1; Rare:31 | ||||
| chr3:38138508-38138811 | Common:2; Rare:106; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:38165456-38165542 | Rare:28 | ||||
| chr3:39051944-39052042 | Common:1; Rare:35 | ||||
| chr3:39107553-39107681 | Common:2; Rare:42 | ||||
| chr3:39153448-39153745 | Common:3; Rare:94 | ||||
| chr3:39383554-39383680 | Rare:32; Clinvar:2 | ||||
| chr3:40309460-40309815 | Common:9; Rare:120 | ||||
| chr3:40457212-40457388 | Common:3; Rare:88 | ||||
| chr3:40524815-40525047 | Common:1; Rare:65 | ||||
| chr3:41200071-41200143 | Rare:24 | ||||
| chr3:42581881-42582137 | Common:3; Rare:80 | ||||
| chr3:42582255-42582260 | |||||
| chr3:42600398-42600485 | Common:1; Rare:32 | ||||
| chr3:42600612-42600757 | Rare:53 |