| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11766690-11767400 | Common:5; Rare:262 | ||||
| chr19:11814122-11814321 | Common:2; Rare:94 | ||||
| chr19:11924958-11925149 | Common:12; Rare:102 | ||||
| chr19:12294694-12294942 | Common:2; Rare:66 | ||||
| chr19:12294863-12294984 | Rare:21 | ||||
| chr19:12401157-12401369 | Common:1; Rare:99 | ||||
| chr19:12551397-12551766 | Common:5; Rare:184 | ||||
| chr19:12610694-12610994 | Rare:193 | ||||
| chr19:12666681-12666851 | Rare:117; Clinvar:8 | ||||
| chr19:12681163-12681596 | Common:4; Rare:270 | ||||
| chr19:12681664-12681965 | Common:4; Rare:308; Clinvar (pathogenic):2 | ||||
| chr19:12696586-12696731 | Rare:123 | ||||
| chr19:12722560-12723030 | Common:4; Rare:142 | ||||
| chr19:12723869-12724089 | Common:2; Rare:100 | ||||
| chr19:12734610-12734907 | Common:2; Rare:205 |