| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:183697676-183697891 | Common:4; Rare:189 | ||||
| chr3:183697990-183698179 | Common:1; Rare:67 | ||||
| chr3:183884816-183885017 | Rare:133 | ||||
| chr3:184017864-184018103 | Common:2; Rare:147 | ||||
| chr3:184134937-184135041 | Common:1; Rare:19 | ||||
| chr3:184135203-184135421 | Common:4; Rare:133; Clinvar:10 | ||||
| chr3:184135450-184135640 | Rare:114; Clinvar:4; Clinvar (pathogenic):4 | ||||
| chr3:184155204-184155538 | Rare:159 | ||||
| chr3:184185856-184186226 | Common:9; Rare:267 | ||||
| chr3:184248746-184249054 | Common:3; Rare:261; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr3:184249234-184249812 | Common:3; Rare:259; Clinvar (benign):1 | ||||
| chr3:184261460-184261852 | Rare:158 | ||||
| chr3:184298941-184299337 | Common:9; Rare:234 | ||||
| chr3:184314300-184314734 | Common:8; Rare:188 | ||||
| chr3:184315132-184315532 | Common:2; Rare:186 |