| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43556835-43557162 | Common:4; Rare:106 | ||||
| chr5:43603102-43603249 | Rare:35 | ||||
| chr5:44808762-44808975 | Common:2; Rare:70 | ||||
| chr5:50441244-50441558 | Common:4; Rare:91 | ||||
| chr5:50666845-50666967 | Common:1; Rare:32 | ||||
| chr5:50667748-50667957 | Common:1; Rare:66 | ||||
| chr5:53109734-53109890 | Common:1; Rare:75; Clinvar:2 | ||||
| chr5:55307663-55308059 | Common:5; Rare:137 | ||||
| chr5:55534719-55534804 | Common:2; Rare:25 | ||||
| chr5:56815212-56815438 | Common:2; Rare:72 | ||||
| chr5:57173544-57173931 | Common:3; Rare:138 | ||||
| chr5:57173966-57174208 | Rare:67 | ||||
| chr5:60945026-60945235 | Common:5; Rare:80; Clinvar:3; Clinvar (benign):5 | ||||
| chr5:61162379-61162676 | Common:1; Rare:79 | ||||
| chr5:62403870-62403997 | Common:3; Rare:40 |