| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16075740-16076064 | Common:7; Rare:90 | ||||
| chr19:16076234-16076568 | Common:2; Rare:100 | ||||
| chr19:16197709-16197983 | Common:3; Rare:88 | ||||
| chr19:16496172-16496424 | Common:2; Rare:60 | ||||
| chr19:16542408-16542620 | Common:2; Rare:59 | ||||
| chr19:16660084-16660384 | Common:3; Rare:114 | ||||
| chr19:16661033-16661203 | Common:1; Rare:56 | ||||
| chr19:16875910-16876087 | Common:2; Rare:46 | ||||
| chr19:16903562-16903848 | Common:1; Rare:101; Clinvar (pathogenic):1 | ||||
| chr19:17215254-17215398 | Common:2; Rare:47 | ||||
| chr19:17215625-17215755 | Rare:33 | ||||
| chr19:17405566-17405847 | Common:6; Rare:48 | ||||
| chr19:17468607-17468790 | Common:1; Rare:31 | ||||
| chr19:18153012-18153284 | Common:1; Rare:92 | ||||
| chr19:18280348-18280599 | Common:1; Rare:89 |