| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:78983628-78983894 | Rare:55 | ||||
| chr5:78984545-78985063 | Common:10; Rare:191; Clinvar:10; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
| chr5:79237039-79237112 | Rare:32 | ||||
| chr5:79237477-79237539 | Rare:22 | ||||
| chr5:79237682-79237733 | Rare:17 | ||||
| chr5:80125455-80125569 | Rare:18 | ||||
| chr5:80247349-80247517 | Common:2; Rare:37 | ||||
| chr5:80256837-80256876 | Rare:8 | ||||
| chr5:80407047-80407149 | Rare:16 | ||||
| chr5:80668154-80668308 | Common:1; Rare:33 | ||||
| chr5:81212282-81212446 | Rare:33 | ||||
| chr5:81749611-81749833 | Common:3; Rare:47 | ||||
| chr5:81779143-81779263 | Common:1; Rare:22 | ||||
| chr5:81851865-81852112 | Common:1; Rare:76 | ||||
| chr5:82273655-82273723 | Common:1; Rare:9 |