| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6740669-6740939 | Common:1; Rare:61 | ||||
| chr19:7294435-7294582 | Common:1; Rare:44 | ||||
| chr19:7395022-7395203 | Common:4; Rare:58 | ||||
| chr19:7488997-7489150 | Common:2; Rare:70 | ||||
| chr19:7535631-7535807 | Common:2; Rare:63 | ||||
| chr19:7629531-7629867 | Common:5; Rare:120; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636981-7637143 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr19:7943629-7943988 | Rare:102 | ||||
| chr19:8308297-8308665 | Common:3; Rare:115 | ||||
| chr19:8321340-8321703 | Common:2; Rare:142 | ||||
| chr19:8364012-8364159 | Common:1; Rare:39 | ||||
| chr19:8390044-8390449 | Common:2; Rare:115 | ||||
| chr19:8514122-8514222 | Common:2; Rare:31 | ||||
| chr19:8526324-8526490 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr19:9140311-9140437 | Rare:36 |