| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31532396-31532675 | Common:4; Rare:79 | ||||
| chr3:31533051-31533293 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr3:31981634-31981826 | Common:1; Rare:48 | ||||
| chr3:32106367-32106714 | Common:4; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502749-32502949 | Rare:60 | ||||
| chr3:32570702-32570928 | Rare:104 | ||||
| chr3:33277312-33277499 | Common:1; Rare:52 | ||||
| chr3:33718061-33718308 | Rare:92 | ||||
| chr3:33798435-33798716 | Common:2; Rare:93 | ||||
| chr3:36944857-36945149 | Common:1; Rare:63 | ||||
| chr3:36993064-36993557 | Common:2; Rare:167; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176315-37176397 | Rare:24 | ||||
| chr3:37243103-37243361 | Common:3; Rare:70 | ||||
| chr3:38024510-38024667 | Common:1; Rare:59 | ||||
| chr3:38029612-38029844 | Common:1; Rare:46 |