| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49513692-49514123 | Common:9; Rare:109 | ||||
| chr19:49556947-49557097 | Rare:57 | ||||
| chr19:49580528-49580694 | Rare:51 | ||||
| chr19:49581248-49581347 | Common:1; Rare:16 | ||||
| chr19:49665577-49666028 | Common:6; Rare:208; Clinvar (pathogenic):1 | ||||
| chr19:49805348-49805537 | Rare:64 | ||||
| chr19:49851045-49851157 | Rare:45 | ||||
| chr19:49854224-49854477 | Common:1; Rare:75 | ||||
| chr19:49857703-49857945 | Common:2; Rare:110 | ||||
| chr19:49867518-49867692 | Common:3; Rare:50; Clinvar:1 | ||||
| chr19:49877268-49877742 | Common:2; Rare:125 | ||||
| chr19:49877835-49878174 | Common:5; Rare:108 | ||||
| chr19:49929074-49929205 | Common:3; Rare:44 | ||||
| chr19:49929430-49929555 | Common:4; Rare:45 | ||||
| chr19:50476392-50476547 | Rare:75 |