| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6372519-6372738 | Common:3; Rare:66 | ||||
| chr19:6373666-6373731 | Common:1; Rare:8 | ||||
| chr19:6415594-6415892 | Common:4; Rare:123 | ||||
| chr19:6416780-6417083 | Common:1; Rare:101 | ||||
| chr19:6733009-6733121 | Rare:37 | ||||
| chr19:6737169-6737325 | Common:1; Rare:45 | ||||
| chr19:6741068-6741281 | Rare:70 | ||||
| chr19:7069653-7069739 | Common:1; Rare:26 | ||||
| chr19:7515943-7516245 | Rare:70 | ||||
| chr19:7522483-7522677 | Common:1; Rare:66; Clinvar:2 | ||||
| chr19:7533823-7534239 | Common:4; Rare:117; Clinvar (benign):2 | ||||
| chr19:7535560-7535792 | Common:3; Rare:84 | ||||
| chr19:7629529-7629899 | Common:5; Rare:129; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7630474-7630657 | Rare:42; Clinvar (benign):1 | ||||
| chr19:7636981-7637182 | Common:2; Rare:59; Clinvar (benign):1 |