| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37779594-37779662 | Rare:11 | ||||
| chr19:38264797-38264893 | Rare:36 | ||||
| chr19:38374407-38374812 | Rare:149 | ||||
| chr19:38618970-38619271 | Common:2; Rare:84 | ||||
| chr19:38647372-38647825 | Common:3; Rare:152 | ||||
| chr19:38724309-38724453 | Rare:61; Clinvar:1 | ||||
| chr19:38831762-38832064 | Common:4; Rare:89; Clinvar (benign):1 | ||||
| chr19:38899517-38900026 | Rare:154 | ||||
| chr19:38930732-38930987 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39084112-39084369 | Rare:68 | ||||
| chr19:39342360-39342509 | Common:2; Rare:46 | ||||
| chr19:39390850-39390930 | Rare:34 | ||||
| chr19:39390982-39391422 | Common:1; Rare:167 | ||||
| chr19:39406706-39406926 | Rare:91 | ||||
| chr19:39435876-39436169 | Common:6; Rare:111 |