| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46000727-46000793 | Rare:15 | ||||
| chr20:46013750-46014019 | Common:3; Rare:62; Clinvar (benign):1 | ||||
| chr20:46020618-46020756 | Common:1; Rare:19 | ||||
| chr20:46058461-46058556 | Rare:17 | ||||
| chr20:46350522-46350772 | Common:1; Rare:52 | ||||
| chr20:47315766-47315949 | Common:1; Rare:31 | ||||
| chr20:47317338-47317643 | Common:1; Rare:62 | ||||
| chr20:47318036-47318309 | Common:1; Rare:42 | ||||
| chr20:47348579-47348642 | Rare:11 | ||||
| chr20:47357697-47357908 | Rare:34 | ||||
| chr20:47359129-47359280 | Rare:33 | ||||
| chr20:47392069-47392283 | Common:2; Rare:37 | ||||
| chr20:47493343-47493358 | Rare:1 | ||||
| chr20:47501205-47501317 | Rare:14 | ||||
| chr20:47575028-47575118 | Rare:10 |