| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49085103-49085492 | Common:3; Rare:153 | ||||
| chr19:49114141-49114405 | Common:4; Rare:60 | ||||
| chr19:49155360-49155529 | Rare:28 | ||||
| chr19:49362375-49362473 | Rare:27 | ||||
| chr19:49451742-49451976 | Common:3; Rare:61 | ||||
| chr19:49453056-49453300 | Common:1; Rare:78 | ||||
| chr19:49513083-49513452 | Common:1; Rare:77 | ||||
| chr19:49527860-49528031 | Common:3; Rare:53 | ||||
| chr19:49528386-49528564 | Rare:57 | ||||
| chr19:49580515-49580670 | Rare:55 | ||||
| chr19:49665718-49666029 | Common:3; Rare:145; Clinvar (pathogenic):1 | ||||
| chr19:49690910-49691138 | Rare:58 | ||||
| chr19:49813267-49813328 | Rare:27 | ||||
| chr19:49877293-49877717 | Common:1; Rare:107 | ||||
| chr19:49929451-49929771 | Common:7; Rare:109 |