| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:8444800-8445008 | Common:3; Rare:90 | ||||
| chr19:8514145-8514223 | Common:1; Rare:22 | ||||
| chr19:9140311-9140442 | Common:1; Rare:36 | ||||
| chr19:9538596-9538690 | Common:1; Rare:27 | ||||
| chr19:9621184-9621525 | Common:3; Rare:96 | ||||
| chr19:9818810-9818841 | Rare:9 | ||||
| chr19:9827828-9827982 | Common:1; Rare:56 | ||||
| chr19:10086629-10087045 | Common:5; Rare:101 | ||||
| chr19:10090906-10091135 | Common:2; Rare:47 | ||||
| chr19:10091216-10091268 | Rare:14 | ||||
| chr19:10091955-10092078 | Rare:28 | ||||
| chr19:10116873-10117151 | Rare:79 | ||||
| chr19:10270955-10271140 | Rare:46 | ||||
| chr19:10333504-10333734 | Rare:75 | ||||
| chr19:10352496-10352825 | Common:5; Rare:77; Clinvar:1; Clinvar (benign):1 |