| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33659062-33659140 | Common:3; Rare:14 | ||||
| chr3:33659506-33659773 | Common:1; Rare:63 | ||||
| chr3:33718061-33718308 | Rare:92 | ||||
| chr3:33798495-33798686 | Common:2; Rare:69 | ||||
| chr3:33799006-33799130 | Rare:39 | ||||
| chr3:36992775-36992943 | Rare:51 | ||||
| chr3:36993051-36993580 | Common:2; Rare:187; Clinvar:32; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr3:36993759-36993840 | Rare:29 | ||||
| chr3:37176241-37176436 | Rare:67 | ||||
| chr3:37243145-37243388 | Common:1; Rare:66 | ||||
| chr3:38024342-38024664 | Common:1; Rare:125 | ||||
| chr3:38165437-38165571 | Rare:46 | ||||
| chr3:38165777-38165860 | Rare:30 | ||||
| chr3:39051883-39052056 | Common:1; Rare:57 | ||||
| chr3:39052457-39052520 | Rare:21 |