| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:39107555-39107698 | Common:3; Rare:45 | ||||
| chr3:39383283-39383659 | Common:3; Rare:81; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:40309491-40309826 | Common:9; Rare:117 | ||||
| chr3:40457227-40457394 | Common:3; Rare:86 | ||||
| chr3:40524812-40525013 | Common:1; Rare:58 | ||||
| chr3:42159936-42160216 | Common:1; Rare:56 | ||||
| chr3:42581898-42582137 | Common:3; Rare:75 | ||||
| chr3:42582292-42582579 | Common:3; Rare:58 | ||||
| chr3:42600372-42600496 | Common:1; Rare:48 | ||||
| chr3:42600533-42601052 | Common:1; Rare:179 | ||||
| chr3:42630774-42631221 | Common:1; Rare:80 | ||||
| chr3:42773206-42773348 | Common:1; Rare:42 | ||||
| chr3:42804407-42804657 | Common:2; Rare:73 | ||||
| chr3:42843692-42844029 | Common:2; Rare:44 | ||||
| chr3:42906005-42906188 | Common:3; Rare:48 |