| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49453473-49453612 | Rare:39 | ||||
| chr19:49496220-49496470 | Common:1; Rare:91 | ||||
| chr19:49513109-49513433 | Common:1; Rare:72 | ||||
| chr19:49527864-49528031 | Common:3; Rare:51 | ||||
| chr19:49556953-49557097 | Rare:55 | ||||
| chr19:49560337-49560647 | Common:2; Rare:48 | ||||
| chr19:49560687-49560898 | Rare:50 | ||||
| chr19:49580534-49580686 | Rare:47 | ||||
| chr19:49662164-49662442 | Common:1; Rare:96 | ||||
| chr19:49665577-49666027 | Common:6; Rare:207; Clinvar (pathogenic):1 | ||||
| chr19:49685772-49686084 | Common:2; Rare:63 | ||||
| chr19:49690980-49691140 | Rare:36 | ||||
| chr19:49808816-49808981 | Rare:55 | ||||
| chr19:49813251-49813328 | Rare:33 | ||||
| chr19:49851045-49851120 | Rare:31 |