| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33097104-33097285 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33114421-33114530 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):3 | ||||
| chr3:36993034-36993564 | Common:2; Rare:180; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:38137074-38137447 | Common:1; Rare:82 | ||||
| chr3:38138569-38138732 | Common:2; Rare:64; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39051779-39052045 | Common:2; Rare:72 | ||||
| chr3:39107545-39107741 | Common:4; Rare:61 | ||||
| chr3:40309448-40309808 | Common:9; Rare:123 | ||||
| chr3:40457196-40457355 | Common:2; Rare:74 | ||||
| chr3:40477059-40477179 | Common:1; Rare:29 | ||||
| chr3:42581892-42582123 | Common:2; Rare:75 | ||||
| chr3:42654120-42654171 | Rare:11 | ||||
| chr3:42773211-42773357 | Common:1; Rare:40 | ||||
| chr3:44861763-44861921 | Common:2; Rare:72 | ||||
| chr3:44976122-44976283 | Common:2; Rare:69 |