| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40425975-40426147 | Common:1; Rare:53 | ||||
| chr19:40576722-40576920 | Common:3; Rare:62 | ||||
| chr19:40751076-40751318 | Common:3; Rare:71 | ||||
| chr19:40778058-40778278 | Common:1; Rare:70 | ||||
| chr19:41218678-41218969 | Common:7; Rare:65 | ||||
| chr19:41264957-41265102 | Common:2; Rare:32 | ||||
| chr19:41364123-41364309 | Rare:59; Clinvar:1 | ||||
| chr19:41397321-41397606 | Common:4; Rare:75 | ||||
| chr19:41860051-41860278 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:41861008-41861209 | Rare:63; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:42075830-42076185 | Rare:98 | ||||
| chr19:42220128-42220349 | Common:2; Rare:62 | ||||
| chr19:43575565-43575800 | Common:1; Rare:50 | ||||
| chr19:43619572-43619686 | Common:1; Rare:33 | ||||
| chr19:43670124-43670324 | Common:2; Rare:53 |