| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10872091-10872410 | Rare:62 | ||||
| chr19:10928618-10928939 | Common:1; Rare:113 | ||||
| chr19:10960602-10960961 | Common:7; Rare:137 | ||||
| chr19:10960967-10961354 | Rare:131; Clinvar (benign):2 | ||||
| chr19:11089060-11089125 | Rare:6 | ||||
| chr19:11089228-11089618 | Rare:79; Clinvar:17; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chr19:11089814-11089910 | Common:1; Rare:17 | ||||
| chr19:11090153-11090662 | Common:2; Rare:149 | ||||
| chr19:11155674-11156228 | Common:4; Rare:148 | ||||
| chr19:11197485-11197707 | Common:1; Rare:67 | ||||
| chr19:11197780-11198030 | Common:2; Rare:71 | ||||
| chr19:11262114-11262439 | Common:1; Rare:70 | ||||
| chr19:11262463-11262636 | Common:1; Rare:50 | ||||
| chr19:11339611-11339847 | Common:4; Rare:62 | ||||
| chr19:11346203-11346597 | Rare:88 |