| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45420338-45420638 | Rare:101; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr20:45791928-45791996 | Rare:25 | ||||
| chr20:45827250-45827504 | Common:1; Rare:41 | ||||
| chr20:45857350-45857593 | Common:3; Rare:63 | ||||
| chr20:45881031-45881234 | Common:2; Rare:46 | ||||
| chr20:45891227-45891342 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:45934416-45934705 | Common:2; Rare:124 | ||||
| chr20:46364391-46364518 | Rare:49 | ||||
| chr20:46406571-46406787 | Common:2; Rare:57 | ||||
| chr20:47356666-47356943 | Rare:65 | ||||
| chr20:47501744-47502019 | Common:1; Rare:97 | ||||
| chr20:49046179-49046354 | Common:3; Rare:51 | ||||
| chr20:49219281-49219449 | Rare:87 | ||||
| chr20:49278038-49278266 | Rare:64 | ||||
| chr20:50113138-50113244 | Common:5; Rare:52 |