| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12484330-12484554 | Common:5; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664075-12664315 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12840448-12840720 | Common:1; Rare:63 | ||||
| chr3:13480029-13480334 | Common:2; Rare:74 | ||||
| chr3:14124661-14125184 | Common:4; Rare:153; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178532-14178870 | Common:2; Rare:175; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651486-14651824 | Rare:101 | ||||
| chr3:14947209-14947563 | Common:4; Rare:156 | ||||
| chr3:15065217-15065356 | Common:2; Rare:59 | ||||
| chr3:15099128-15099283 | Rare:37 | ||||
| chr3:15206019-15206278 | Rare:95 | ||||
| chr3:15427471-15427629 | Common:1; Rare:57 | ||||
| chr3:15601516-15602046 | Common:6; Rare:246; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:15796027-15796171 | Common:3; Rare:25 | ||||
| chr3:15796840-15796950 | Rare:16 |