| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1633941-1634051 | Common:2; Rare:34 | ||||
| chr5:1883374-1883436 | Rare:12 | ||||
| chr5:1884143-1884499 | Common:1; Rare:66 | ||||
| chr5:1936497-1936757 | Common:1; Rare:50 | ||||
| chr5:1973726-1973947 | Common:2; Rare:44 | ||||
| chr5:3601379-3601576 | Rare:42 | ||||
| chr5:4561158-4561225 | Rare:9 | ||||
| chr5:8457544-8457761 | Common:2; Rare:79 | ||||
| chr5:10254416-10254841 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr5:10397320-10397365 | Rare:5 | ||||
| chr5:13567855-13568169 | Common:1; Rare:48 | ||||
| chr5:14145227-14145584 | Common:3; Rare:101 | ||||
| chr5:14145944-14146246 | Rare:47 | ||||
| chr5:14159351-14159557 | Common:1; Rare:32 | ||||
| chr5:14169052-14169217 | Common:2; Rare:30 |