| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:11225808-11226027 | Rare:38 | ||||
| chr3:11272227-11272427 | Common:1; Rare:44 | ||||
| chr3:11719423-11719579 | Rare:49 | ||||
| chr3:12484333-12484535 | Common:5; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:12664075-12664309 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13480040-13480330 | Common:2; Rare:67 | ||||
| chr3:14124723-14125156 | Common:4; Rare:125; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14170460-14170749 | Common:4; Rare:71; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14178532-14178873 | Common:2; Rare:176; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402479-14402722 | Rare:57 | ||||
| chr3:14651453-14651847 | Rare:123 | ||||
| chr3:14947233-14947583 | Common:4; Rare:159 | ||||
| chr3:15206003-15206279 | Rare:102 | ||||
| chr3:15427471-15427635 | Common:1; Rare:60 | ||||
| chr3:15601506-15601804 | Common:4; Rare:124; Clinvar:1 |