| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184176811-184177067 | Common:1; Rare:55 | ||||
| chr3:184189101-184189428 | Common:5; Rare:69 | ||||
| chr3:184189583-184189932 | Rare:125; Clinvar:1 | ||||
| chr3:184248749-184249015 | Rare:121; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:184249451-184249749 | Common:1; Rare:85 | ||||
| chr3:184299109-184299419 | Common:4; Rare:90 | ||||
| chr3:184299860-184299968 | Common:1; Rare:37 | ||||
| chr3:184300257-184300291 | Rare:11 | ||||
| chr3:184306747-184306893 | Rare:38 | ||||
| chr3:184307326-184308017 | Common:1; Rare:177 | ||||
| chr3:184314411-184314671 | Common:3; Rare:76 | ||||
| chr3:184315008-184315266 | Rare:70 | ||||
| chr3:184320691-184320969 | Rare:74 | ||||
| chr3:184325268-184325639 | Common:1; Rare:95 | ||||
| chr3:184331476-184331778 | Common:6; Rare:86 |