| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37779546-37779662 | Rare:26 | ||||
| chr19:38264331-38264676 | Common:5; Rare:87 | ||||
| chr19:38315907-38316119 | Rare:60 | ||||
| chr19:38336278-38336470 | Common:2; Rare:44 | ||||
| chr19:38374407-38374844 | Rare:169 | ||||
| chr19:38618840-38619252 | Common:4; Rare:123 | ||||
| chr19:38736863-38737158 | Common:5; Rare:53 | ||||
| chr19:38831709-38832064 | Common:5; Rare:116; Clinvar (benign):1 | ||||
| chr19:38852319-38852584 | Rare:66 | ||||
| chr19:38899513-38900033 | Rare:158 | ||||
| chr19:38930715-38931013 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975681-38975845 | Common:1; Rare:37 | ||||
| chr19:39390850-39391431 | Common:1; Rare:218 | ||||
| chr19:39406679-39406880 | Rare:72 | ||||
| chr19:39435850-39436154 | Common:6; Rare:109 |