| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40646201-40646417 | Common:3; Rare:42 | ||||
| chr19:40646440-40647000 | Common:3; Rare:125 | ||||
| chr19:40662820-40663180 | Common:3; Rare:89 | ||||
| chr19:40663615-40663733 | Rare:24 | ||||
| chr19:40718969-40719083 | Common:1; Rare:23 | ||||
| chr19:40798190-40798367 | Rare:49 | ||||
| chr19:40810870-40811220 | Common:4; Rare:89 | ||||
| chr19:41176148-41176495 | Common:4; Rare:72 | ||||
| chr19:41225800-41226040 | Common:2; Rare:60 | ||||
| chr19:41351582-41351757 | Common:2; Rare:31 | ||||
| chr19:41352582-41352736 | Common:1; Rare:50 | ||||
| chr19:41352937-41353146 | Common:4; Rare:67; Clinvar (benign):2 | ||||
| chr19:41380260-41380650 | Common:1; Rare:66 | ||||
| chr19:41449220-41449624 | Common:1; Rare:90 | ||||
| chr19:41501606-41501733 | Rare:23 |