| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12556864-12557153 | Common:5; Rare:93 | ||||
| chr3:12663450-12663654 | Common:2; Rare:63 | ||||
| chr3:12663816-12663971 | Rare:43; Clinvar:4; Clinvar (benign):3 | ||||
| chr3:12664080-12664225 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:12840635-12840888 | Common:2; Rare:41 | ||||
| chr3:13480089-13480436 | Common:2; Rare:82 | ||||
| chr3:14124683-14125184 | Common:4; Rare:147; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14170436-14170641 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr3:14178466-14178870 | Common:3; Rare:194; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402326-14402632 | Common:1; Rare:82 | ||||
| chr3:14651468-14651847 | Rare:120 | ||||
| chr3:14947133-14947591 | Common:5; Rare:195 | ||||
| chr3:14948105-14948663 | Common:2; Rare:198 | ||||
| chr3:15099119-15099310 | Rare:47 | ||||
| chr3:15206008-15206351 | Common:1; Rare:123 |