| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12484389-12484560 | Common:2; Rare:54; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12556905-12557164 | Common:5; Rare:90 | ||||
| chr3:12664080-12664331 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:13480018-13480339 | Common:2; Rare:80 | ||||
| chr3:14124685-14125151 | Common:4; Rare:136; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178881 | Common:2; Rare:166; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402437-14402695 | Rare:61 | ||||
| chr3:14651463-14651828 | Rare:110 | ||||
| chr3:14947236-14947569 | Common:4; Rare:153 | ||||
| chr3:14948024-14948140 | Rare:61 | ||||
| chr3:14948398-14948675 | Common:2; Rare:88 | ||||
| chr3:15065059-15065389 | Common:2; Rare:118 | ||||
| chr3:15099109-15099283 | Rare:43 | ||||
| chr3:15206043-15206278 | Rare:91 | ||||
| chr3:15341361-15341590 | Common:1; Rare:40 |