| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19516147-19516261 | Rare:67; Clinvar (pathogenic):1 | ||||
| chr19:19628210-19628316 | Rare:24 | ||||
| chr19:19668620-19668792 | Rare:39 | ||||
| chr19:19733084-19733263 | Common:2; Rare:47 | ||||
| chr19:19821700-19821866 | Common:1; Rare:56 | ||||
| chr19:20923119-20923325 | Rare:56 | ||||
| chr19:21396948-21397128 | Rare:37 | ||||
| chr19:21505474-21505621 | Rare:33 | ||||
| chr19:29213138-29213233 | Common:1; Rare:36 | ||||
| chr19:29606207-29606315 | Rare:39 | ||||
| chr19:29665253-29665444 | Common:4; Rare:70 | ||||
| chr19:32971903-32972262 | Common:4; Rare:102 | ||||
| chr19:33064865-33065043 | Common:1; Rare:62 | ||||
| chr19:33373545-33373845 | Common:2; Rare:97 | ||||
| chr19:33521765-33521956 | Common:1; Rare:57; Clinvar:3 |