| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33113827-33114094 | Common:4; Rare:139; Clinvar:2; Clinvar (benign):4 | ||||
| chr3:33114250-33114750 | Common:3; Rare:200; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr3:33277220-33277495 | Common:4; Rare:116 | ||||
| chr3:33440020-33440868 | Common:8; Rare:433 | ||||
| chr3:33440907-33441065 | Rare:29 | ||||
| chr3:33718047-33718320 | Rare:155 | ||||
| chr3:33798434-33798695 | Common:4; Rare:130 | ||||
| chr3:33798710-33798930 | Common:2; Rare:134 | ||||
| chr3:36380367-36380535 | Common:1; Rare:61 | ||||
| chr3:36908435-36908571 | Common:1; Rare:29 | ||||
| chr3:36992609-36993009 | Common:2; Rare:185 | ||||
| chr3:36993060-36993615 | Common:4; Rare:363; Clinvar:67; Clinvar (benign):31; Clinvar (pathogenic):7 | ||||
| chr3:37176241-37176465 | Common:1; Rare:131 | ||||
| chr3:37243146-37243429 | Common:2; Rare:120 | ||||
| chr3:37243600-37244080 | Common:6; Rare:274 |