| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35454710-35454847 | Common:2; Rare:38 | ||||
| chr20:35455042-35455405 | Common:1; Rare:115 | ||||
| chr20:35455488-35455615 | Rare:33 | ||||
| chr20:35541823-35542249 | Common:3; Rare:150 | ||||
| chr20:35542343-35542557 | Rare:72 | ||||
| chr20:35619316-35619481 | Rare:41 | ||||
| chr20:35632005-35632174 | Common:5; Rare:48 | ||||
| chr20:35664770-35665027 | Common:1; Rare:68 | ||||
| chr20:35699280-35699498 | Rare:75; Clinvar (benign):3 | ||||
| chr20:35742140-35742664 | Common:6; Rare:165 | ||||
| chr20:35771823-35772077 | Common:2; Rare:82 | ||||
| chr20:36154452-36154686 | Rare:41 | ||||
| chr20:36236403-36236536 | Common:1; Rare:35 | ||||
| chr20:36573211-36573750 | Common:2; Rare:198 | ||||
| chr20:36574394-36574620 | Rare:75 |