| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9668982-9669151 | Rare:26 | ||||
| chr19:9683605-9683776 | Common:1; Rare:42 | ||||
| chr19:9749702-9749919 | Common:1; Rare:40 | ||||
| chr19:10652447-10652643 | Common:1; Rare:32 | ||||
| chr19:11437948-11438124 | Rare:59; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:12533218-12533260 | Rare:6 | ||||
| chr19:12649885-12650248 | Common:3; Rare:115; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:12698963-12699246 | Rare:61 | ||||
| chr19:12924152-12924502 | Common:1; Rare:94 | ||||
| chr19:13167558-13167715 | Rare:44 | ||||
| chr19:13832318-13832455 | Common:2; Rare:20 | ||||
| chr19:13834459-13834524 | Rare:6 | ||||
| chr19:14167116-14167393 | Common:1; Rare:58 | ||||
| chr19:16077650-16077924 | Common:4; Rare:59 | ||||
| chr19:16078926-16079054 | Rare:15 |