| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:16542416-16542603 | Common:2; Rare:52 | ||||
| chr19:16660112-16660392 | Common:3; Rare:102 | ||||
| chr19:17215245-17215398 | Common:2; Rare:51 | ||||
| chr19:17215617-17215760 | Common:1; Rare:38 | ||||
| chr19:17405577-17405847 | Common:6; Rare:46 | ||||
| chr19:18152990-18153283 | Common:1; Rare:94 | ||||
| chr19:18323010-18323253 | Common:3; Rare:84 | ||||
| chr19:18683513-18683688 | Common:1; Rare:56 | ||||
| chr19:18919349-18919740 | Common:2; Rare:138 | ||||
| chr19:19033482-19033649 | Common:2; Rare:51 | ||||
| chr19:19033837-19033916 | Common:1; Rare:19 | ||||
| chr19:19192122-19192195 | Common:1; Rare:28 | ||||
| chr19:19192583-19192927 | Common:2; Rare:91 | ||||
| chr19:19320496-19320802 | Common:4; Rare:99 | ||||
| chr19:19516093-19516274 | Rare:110; Clinvar (pathogenic):1 |