| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42217671-42217975 | Common:2; Rare:108 | ||||
| chr19:42220092-42220356 | Common:2; Rare:76 | ||||
| chr19:42268211-42268587 | Rare:79 | ||||
| chr19:42302394-42302560 | Rare:42 | ||||
| chr19:42325394-42325676 | Rare:72 | ||||
| chr19:42423526-42423753 | Common:4; Rare:81 | ||||
| chr19:43527174-43527310 | Common:4; Rare:54; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:43575483-43575713 | Common:1; Rare:71 | ||||
| chr19:43580483-43580655 | Common:3; Rare:26 | ||||
| chr19:43596101-43596433 | Common:2; Rare:103 | ||||
| chr19:43619498-43619552 | Rare:14 | ||||
| chr19:43619571-43619686 | Common:1; Rare:33 | ||||
| chr19:43670111-43670320 | Common:2; Rare:57 | ||||
| chr19:43754840-43755088 | Common:3; Rare:98 | ||||
| chr19:43780957-43781170 | Rare:43 |