| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7522609-7522688 | Rare:32; Clinvar:2 | ||||
| chr19:7535574-7535760 | Common:3; Rare:66 | ||||
| chr19:7629529-7629859 | Common:5; Rare:117; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636941-7637152 | Common:3; Rare:60; Clinvar (benign):1 | ||||
| chr19:7903542-7903889 | Rare:105 | ||||
| chr19:7920255-7920364 | Rare:51 | ||||
| chr19:7943632-7943988 | Rare:100 | ||||
| chr19:8005520-8005821 | Common:1; Rare:105 | ||||
| chr19:8308290-8308633 | Common:3; Rare:111; Clinvar (benign):1 | ||||
| chr19:8321335-8321703 | Common:2; Rare:146 | ||||
| chr19:8364049-8364167 | Common:1; Rare:31 | ||||
| chr19:8390048-8390412 | Common:1; Rare:103 | ||||
| chr19:8444807-8445052 | Common:2; Rare:114 | ||||
| chr19:8526349-8526479 | Rare:42; Clinvar (benign):1 | ||||
| chr19:8832240-8832358 | Common:1; Rare:43 |