| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7528585-7528902 | Common:3; Rare:109; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chr19:7535571-7535800 | Common:3; Rare:84 | ||||
| chr19:7539943-7540211 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:7541232-7541378 | Rare:46; Clinvar:1 | ||||
| chr19:7629529-7629847 | Common:5; Rare:115; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636973-7637152 | Common:2; Rare:55; Clinvar (benign):1 | ||||
| chr19:7639656-7639769 | Rare:32 | ||||
| chr19:7642106-7642208 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:7676967-7677139 | Rare:40 | ||||
| chr19:7677759-7678240 | Common:5; Rare:109 | ||||
| chr19:7678241-7678510 | Common:1; Rare:89 | ||||
| chr19:7702049-7702283 | Common:2; Rare:49 | ||||
| chr19:7903542-7903861 | Rare:97 | ||||
| chr19:7920188-7920364 | Rare:68 | ||||
| chr19:7943630-7943997 | Rare:103 |