| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74597570-74597915 | Common:2; Rare:92 | ||||
| chr18:76822256-76822638 | Common:11; Rare:103 | ||||
| chr18:79679276-79679490 | Rare:109 | ||||
| chr18:79988356-79988651 | Common:3; Rare:106; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:507468-507506 | Rare:11 | ||||
| chr19:572326-572649 | Rare:174 | ||||
| chr19:633520-633710 | Common:8; Rare:86 | ||||
| chr19:663126-663446 | Common:3; Rare:128 | ||||
| chr19:708788-709149 | Common:3; Rare:101 | ||||
| chr19:859100-859467 | Common:3; Rare:93 | ||||
| chr19:859543-859700 | Rare:55 | ||||
| chr19:893165-893484 | Common:3; Rare:133 | ||||
| chr19:913153-913289 | Rare:44 | ||||
| chr19:984277-984356 | Rare:24 | ||||
| chr19:1026518-1026676 | Rare:68 |