| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38850927-38850954 | Rare:8 | ||||
| chr19:38851271-38851514 | Rare:64 | ||||
| chr19:38851815-38852189 | Common:4; Rare:132 | ||||
| chr19:38852239-38852372 | Rare:40 | ||||
| chr19:38852554-38852812 | Common:2; Rare:61 | ||||
| chr19:38899481-38899749 | Rare:77 | ||||
| chr19:38899813-38900113 | Rare:89 | ||||
| chr19:38900148-38900316 | Common:1; Rare:36 | ||||
| chr19:38930307-38930558 | Common:1; Rare:95; Clinvar (benign):1 | ||||
| chr19:38930687-38931070 | Common:4; Rare:111; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:38931079-38931205 | Common:2; Rare:31 | ||||
| chr19:38975412-38975557 | Rare:26 | ||||
| chr19:38975637-38975965 | Common:1; Rare:75 | ||||
| chr19:38976056-38976133 | Rare:17 | ||||
| chr19:38976281-38976382 | Rare:21 |