| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9818809-9818877 | Rare:28 | ||||
| chr19:10270926-10271126 | Rare:47 | ||||
| chr19:10333503-10333709 | Rare:66 | ||||
| chr19:10403462-10403755 | Rare:124 | ||||
| chr19:10502713-10502992 | Rare:78 | ||||
| chr19:10960712-10961059 | Common:3; Rare:136 | ||||
| chr19:11089281-11089539 | Rare:51; Clinvar:12; Clinvar (pathogenic):1 | ||||
| chr19:11197509-11197625 | Common:1; Rare:30 | ||||
| chr19:11559195-11559389 | Common:1; Rare:61 | ||||
| chr19:11738894-11739252 | Common:4; Rare:95 | ||||
| chr19:12484783-12485036 | Common:1; Rare:60 | ||||
| chr19:12551452-12551690 | Common:2; Rare:61 | ||||
| chr19:12610723-12610994 | Rare:93 | ||||
| chr19:12666683-12666838 | Rare:63; Clinvar:4 | ||||
| chr19:12696611-12696707 | Rare:43 |