| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23805613-23805935 | Common:3; Rare:62 | ||||
| chr3:23916909-23917204 | Rare:112 | ||||
| chr3:28241474-28241672 | Common:1; Rare:71 | ||||
| chr3:28348789-28349052 | Common:2; Rare:84 | ||||
| chr3:29281011-29281076 | Rare:9 | ||||
| chr3:32106418-32106633 | Common:4; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32570766-32570948 | Common:1; Rare:85 | ||||
| chr3:33097104-33097285 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33798521-33798660 | Common:2; Rare:49 | ||||
| chr3:36993126-36993539 | Common:2; Rare:125; Clinvar:25; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr3:37243162-37243310 | Common:1; Rare:35 | ||||
| chr3:40457204-40457368 | Common:2; Rare:79 | ||||
| chr3:42581900-42582106 | Common:2; Rare:67 | ||||
| chr3:42600582-42600703 | Rare:44 | ||||
| chr3:42804442-42804657 | Common:2; Rare:63 |