| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12881897-12882051 | Rare:27 | ||||
| chr19:12890684-12890728 | Rare:4 | ||||
| chr19:12890739-12891229 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:12919197-12919476 | Common:2; Rare:146 | ||||
| chr19:12933620-12933877 | Common:1; Rare:76 | ||||
| chr19:12938012-12938152 | Rare:31 | ||||
| chr19:12938171-12938212 | Rare:3 | ||||
| chr19:12938233-12938808 | Common:7; Rare:224 | ||||
| chr19:12943551-12943857 | Rare:123 | ||||
| chr19:12945819-12945949 | Common:1; Rare:52 | ||||
| chr19:12945975-12946045 | Rare:23 | ||||
| chr19:12946149-12946420 | Rare:65 | ||||
| chr19:12957149-12957339 | Rare:59 | ||||
| chr19:12965462-12965561 | Rare:20 | ||||
| chr19:12995408-12995616 | Rare:57 |