| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19034367-19034447 | Common:2; Rare:14 | ||||
| chr19:19063422-19063824 | Common:1; Rare:142 | ||||
| chr19:19064153-19064283 | Common:1; Rare:25 | ||||
| chr19:19138359-19138655 | Common:3; Rare:88 | ||||
| chr19:19170217-19170446 | Common:2; Rare:54 | ||||
| chr19:19192095-19192318 | Common:1; Rare:68 | ||||
| chr19:19192533-19192973 | Common:2; Rare:117 | ||||
| chr19:19193123-19193178 | Rare:4 | ||||
| chr19:19203132-19203151 | Rare:4 | ||||
| chr19:19203288-19203540 | Common:1; Rare:69 | ||||
| chr19:19320385-19320927 | Common:8; Rare:234 | ||||
| chr19:19385224-19385384 | Rare:52 | ||||
| chr19:19385400-19386120 | Common:1; Rare:207 | ||||
| chr19:19405419-19405873 | Common:4; Rare:139 | ||||
| chr19:19515929-19516502 | Common:3; Rare:258; Clinvar:1; Clinvar (pathogenic):1 |