| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43602852-43603277 | Rare:103 | ||||
| chr5:44808711-44808982 | Common:2; Rare:94 | ||||
| chr5:50667210-50667415 | Common:1; Rare:65 | ||||
| chr5:50667542-50667570 | Rare:13 | ||||
| chr5:50667776-50667957 | Common:1; Rare:58 | ||||
| chr5:52787813-52788453 | Common:2; Rare:151 | ||||
| chr5:53109710-53109899 | Common:1; Rare:97; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310513-54310711 | Rare:63 | ||||
| chr5:55307631-55308035 | Common:5; Rare:141 | ||||
| chr5:55534583-55534844 | Common:3; Rare:84 | ||||
| chr5:55534938-55535179 | Common:1; Rare:82 | ||||
| chr5:55994782-55995184 | Common:1; Rare:131 | ||||
| chr5:56952100-56952390 | Rare:109 | ||||
| chr5:57173608-57174147 | Common:2; Rare:182 | ||||
| chr5:58460072-58460222 | Common:4; Rare:55 |