| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48835833-48835964 | Common:1; Rare:36 | ||||
| chr19:48918699-48919080 | Common:4; Rare:127 | ||||
| chr19:48954596-48954922 | Common:1; Rare:115 | ||||
| chr19:48965240-48965609 | Rare:115; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48993259-48993575 | Common:3; Rare:139; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:49085103-49085492 | Common:3; Rare:153 | ||||
| chr19:49155388-49155563 | Rare:32 | ||||
| chr19:49335390-49335462 | Common:1; Rare:16 | ||||
| chr19:49362375-49362487 | Rare:34 | ||||
| chr19:49453094-49453313 | Common:1; Rare:70 | ||||
| chr19:49453480-49453639 | Common:1; Rare:47 | ||||
| chr19:49496161-49496470 | Common:1; Rare:108 | ||||
| chr19:49513137-49513414 | Common:1; Rare:68 | ||||
| chr19:49580515-49580650 | Rare:49 | ||||
| chr19:49641886-49642233 | Rare:102 |