| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:4493081-4493557 | Common:10; Rare:907; Clinvar:8; Clinvar (benign):6 | ||||
| chr3:4813859-4814259 | Common:3; Rare:81 | ||||
| chr3:4814230-4814889 | Common:53; Rare:780; Clinvar:10; Clinvar (benign):24; Clinvar (pathogenic):6 | ||||
| chr3:4814880-4815040 | Common:2; Rare:42 | ||||
| chr3:4815012-4815268 | Common:1; Rare:52; Clinvar (benign):2 | ||||
| chr3:4978420-4981392 | Common:75; Rare:2936 | ||||
| chr3:5121995-5122405 | Common:6; Rare:426 | ||||
| chr3:5187180-5187770 | Common:43; Rare:1183 | ||||
| chr3:5187898-5188573 | Common:2; Rare:412 | ||||
| chr3:5188586-5189566 | Common:8; Rare:291 | ||||
| chr3:5194851-5195034 | Common:1; Rare:67 | ||||
| chr3:6769751-6770244 | Common:59; Rare:727 | ||||
| chr3:8962718-8963118 | Common:4; Rare:62 | ||||
| chr3:8963185-8963901 | Common:28; Rare:793 | ||||
| chr3:9362652-9363853 | Common:23; Rare:927 |