| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:133661796-133662024 | Rare:105 | ||||
| chr3:133746157-133746492 | Common:4; Rare:134; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:133748120-133748780 | Common:1; Rare:203; Clinvar:6 | ||||
| chr3:133805525-133805864 | Common:2; Rare:187 | ||||
| chr3:134250090-134250520 | Common:4; Rare:149 | ||||
| chr3:134250760-134250899 | Common:2; Rare:91 | ||||
| chr3:134485921-134486260 | Common:6; Rare:165 | ||||
| chr3:136195640-136196130 | Common:4; Rare:305 | ||||
| chr3:136196232-136196483 | Common:1; Rare:155 | ||||
| chr3:136196522-136196909 | Rare:152 | ||||
| chr3:136250224-136250421 | Common:6; Rare:160; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr3:136250460-136250810 | Common:6; Rare:199; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:136255551-136255956 | Common:2; Rare:149; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:136752214-136752751 | Common:3; Rare:303 | ||||
| chr3:136818928-136819228 | Common:8; Rare:245 |