| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49496135-49496496 | Common:1; Rare:129 | ||||
| chr19:49513124-49513479 | Common:1; Rare:78 | ||||
| chr19:49527854-49528031 | Common:3; Rare:56 | ||||
| chr19:49580527-49580686 | Rare:52 | ||||
| chr19:49581238-49581428 | Common:1; Rare:37 | ||||
| chr19:49641826-49642054 | Rare:66 | ||||
| chr19:49665577-49666034 | Common:6; Rare:209; Clinvar (pathogenic):1 | ||||
| chr19:49690980-49691138 | Rare:36 | ||||
| chr19:49808716-49808926 | Common:1; Rare:77; Clinvar:1 | ||||
| chr19:49851045-49851130 | Rare:35 | ||||
| chr19:49854236-49854463 | Common:1; Rare:67 | ||||
| chr19:49858274-49858599 | Common:2; Rare:111 | ||||
| chr19:49867513-49867621 | Common:2; Rare:36; Clinvar:1 | ||||
| chr19:49877211-49877730 | Common:2; Rare:130 | ||||
| chr19:49929172-49929205 | Common:1; Rare:11 |