| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37993919-37994152 | Common:1; Rare:60 | ||||
| chr3:37998411-37998666 | Rare:51 | ||||
| chr3:37998780-37998818 | Rare:2 | ||||
| chr3:38003904-38004275 | Common:2; Rare:84 | ||||
| chr3:38008072-38008239 | Rare:63 | ||||
| chr3:38024447-38024674 | Common:1; Rare:86 | ||||
| chr3:38029612-38029940 | Common:2; Rare:65 | ||||
| chr3:38138596-38138811 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:38165443-38165777 | Common:1; Rare:110 | ||||
| chr3:39051938-39052056 | Common:1; Rare:44 | ||||
| chr3:39088044-39088233 | Rare:50 | ||||
| chr3:39107537-39107730 | Common:4; Rare:61 | ||||
| chr3:39153439-39153750 | Common:3; Rare:98 | ||||
| chr3:39383272-39383437 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383561-39383733 | Rare:44; Clinvar:3 |