| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:14518382-14518785 | Common:6; Rare:158 | ||||
| chr19:14529238-14529706 | Common:1; Rare:196 | ||||
| chr19:15049370-15049645 | Common:3; Rare:50 | ||||
| chr19:15055153-15055533 | Common:3; Rare:115; Clinvar (pathogenic):1 | ||||
| chr19:15331858-15332218 | Common:2; Rare:115 | ||||
| chr19:15508373-15508566 | Common:1; Rare:46 | ||||
| chr19:16067429-16067817 | Common:3; Rare:115 | ||||
| chr19:16076179-16076670 | Common:2; Rare:138 | ||||
| chr19:16185219-16185494 | Common:1; Rare:88 | ||||
| chr19:16496102-16496424 | Common:2; Rare:97 | ||||
| chr19:16542386-16542636 | Common:2; Rare:84 | ||||
| chr19:16660102-16660384 | Common:3; Rare:106 | ||||
| chr19:16661078-16661189 | Common:1; Rare:37 | ||||
| chr19:17215263-17215411 | Common:2; Rare:55 | ||||
| chr19:17215609-17215837 | Common:3; Rare:73 |