| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34428145-34428545 | Common:9; Rare:554 | ||||
| chr19:34428655-34429067 | Common:10; Rare:203 | ||||
| chr19:34677351-34677829 | Common:30; Rare:489 | ||||
| chr19:34733790-34734317 | Common:12; Rare:524 | ||||
| chr19:34734340-34734751 | Common:7; Rare:340 | ||||
| chr19:34734760-34735170 | Rare:111 | ||||
| chr19:34773074-34773474 | Common:9; Rare:244 | ||||
| chr19:34926580-34927095 | Common:11; Rare:474 | ||||
| chr19:34963780-34964601 | Common:7; Rare:366 | ||||
| chr19:34994914-34995314 | Common:5; Rare:158 | ||||
| chr19:34999296-34999740 | Common:6; Rare:191 | ||||
| chr19:34999668-35001276 | Common:18; Rare:957 | ||||
| chr19:35030180-35030845 | Common:4; Rare:354; Clinvar:6; Clinvar (benign):8 | ||||
| chr19:35040820-35041460 | Common:22; Rare:454 | ||||
| chr19:35141138-35141604 | Common:32; Rare:480 |