| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38975724-38975844 | Common:1; Rare:25 | ||||
| chr19:39342404-39342511 | Common:2; Rare:41 | ||||
| chr19:39390850-39390897 | Rare:18 | ||||
| chr19:39391025-39391431 | Common:1; Rare:164 | ||||
| chr19:39406721-39406852 | Rare:54 | ||||
| chr19:39435894-39436155 | Common:4; Rare:98 | ||||
| chr19:39445338-39445805 | Common:5; Rare:146 | ||||
| chr19:39480561-39480931 | Common:3; Rare:172; Clinvar (pathogenic):1 | ||||
| chr19:39846294-39846531 | Common:1; Rare:114 | ||||
| chr19:39970969-39971226 | Common:2; Rare:71 | ||||
| chr19:39996956-39997095 | Common:4; Rare:49 | ||||
| chr19:40056168-40056243 | Rare:13 | ||||
| chr19:40090878-40090964 | Common:1; Rare:23 | ||||
| chr19:40285221-40285479 | Common:1; Rare:90 | ||||
| chr19:40348513-40348720 | Common:3; Rare:64 |