| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40524832-40524984 | Common:1; Rare:37 | ||||
| chr3:42581881-42582137 | Common:3; Rare:80 | ||||
| chr3:42600361-42600750 | Common:2; Rare:155 | ||||
| chr3:42600902-42601004 | Rare:41 | ||||
| chr3:42630892-42631213 | Common:1; Rare:53 | ||||
| chr3:42653541-42653697 | Rare:35 | ||||
| chr3:42773206-42773332 | Common:1; Rare:40 | ||||
| chr3:42804278-42804657 | Common:2; Rare:104 | ||||
| chr3:43690759-43690954 | Common:1; Rare:92; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:43691555-43691633 | Common:1; Rare:13 | ||||
| chr3:44338086-44338180 | Common:2; Rare:34 | ||||
| chr3:44338694-44338807 | Common:3; Rare:40 | ||||
| chr3:44477628-44477752 | Common:1; Rare:26 | ||||
| chr3:44624898-44625085 | Common:2; Rare:57 | ||||
| chr3:44712418-44712720 | Common:2; Rare:85 |