| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49590156-49590342 | Common:2; Rare:69 | ||||
| chr19:49665762-49666029 | Common:2; Rare:132; Clinvar (pathogenic):1 | ||||
| chr19:49813251-49813341 | Rare:38 | ||||
| chr19:49851058-49851162 | Rare:39 | ||||
| chr19:49857502-49857775 | Common:3; Rare:101 | ||||
| chr19:49867216-49867467 | Common:2; Rare:68; Clinvar (benign):2 | ||||
| chr19:49867527-49867650 | Common:2; Rare:38; Clinvar:1 | ||||
| chr19:49876617-49876715 | Rare:42 | ||||
| chr19:49877271-49877717 | Common:2; Rare:111 | ||||
| chr19:49877836-49878136 | Common:5; Rare:93 | ||||
| chr19:49929111-49929205 | Common:3; Rare:32 | ||||
| chr19:49929408-49929566 | Common:4; Rare:57 | ||||
| chr19:49929923-49930166 | Common:1; Rare:47 | ||||
| chr19:50025316-50025722 | Common:7; Rare:140 | ||||
| chr19:50377603-50377825 | Common:1; Rare:90 |