| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6720462-6720709 | Rare:62; Clinvar (benign):2 | ||||
| chr19:6720711-6720990 | Rare:61 | ||||
| chr19:7395022-7395207 | Common:4; Rare:58 | ||||
| chr19:7488988-7489166 | Common:2; Rare:81 | ||||
| chr19:7535574-7535791 | Common:3; Rare:79 | ||||
| chr19:7629511-7629848 | Common:5; Rare:124; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7637002-7637176 | Common:2; Rare:53; Clinvar (benign):1 | ||||
| chr19:7903508-7903923 | Common:2; Rare:135 | ||||
| chr19:7920143-7920375 | Rare:80 | ||||
| chr19:7943630-7943997 | Rare:103 | ||||
| chr19:8005520-8005822 | Common:1; Rare:106 | ||||
| chr19:8308291-8308639 | Common:2; Rare:112 | ||||
| chr19:8321322-8321703 | Common:2; Rare:153 | ||||
| chr19:8363995-8364162 | Common:1; Rare:43 | ||||
| chr19:8390038-8390445 | Common:2; Rare:115 |