| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49093297-49093311 | Rare:4 | ||||
| chr3:49093564-49093752 | Common:1; Rare:66 | ||||
| chr3:49093914-49094138 | Rare:56 | ||||
| chr3:49099587-49099846 | Rare:91; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr3:49100112-49100243 | Rare:43; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:49104616-49104919 | Common:1; Rare:124; Clinvar:3; Clinvar (benign):7 | ||||
| chr3:49110649-49110775 | Rare:35 | ||||
| chr3:49120764-49121366 | Common:2; Rare:162; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:49125005-49125359 | Common:2; Rare:113; Clinvar:3; Clinvar (benign):4 | ||||
| chr3:49128782-49129093 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:49132797-49133117 | Rare:75; Clinvar:3 | ||||
| chr3:49166268-49166442 | Common:1; Rare:46 | ||||
| chr3:49358129-49358484 | Common:4; Rare:183 | ||||
| chr3:49411888-49412450 | Common:2; Rare:205 | ||||
| chr3:49429295-49429348 | Rare:11 |