| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16077193-16077343 | Common:1; Rare:31 | ||||
| chr19:16077365-16077483 | Rare:42 | ||||
| chr19:16077511-16077566 | Common:2; Rare:9 | ||||
| chr19:16093591-16094020 | Rare:93 | ||||
| chr19:16111251-16111694 | Common:9; Rare:130 | ||||
| chr19:16111733-16111960 | Common:1; Rare:52 | ||||
| chr19:16185092-16185521 | Common:1; Rare:132 | ||||
| chr19:16197590-16197992 | Common:4; Rare:116 | ||||
| chr19:16198012-16198169 | Rare:57 | ||||
| chr19:16324438-16324714 | Common:3; Rare:83 | ||||
| chr19:16324742-16324930 | Rare:55 | ||||
| chr19:16471825-16472245 | Common:5; Rare:131 | ||||
| chr19:16495952-16496539 | Common:4; Rare:178; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:16542183-16542685 | Common:2; Rare:166 | ||||
| chr19:16542782-16542889 | Rare:32 |