| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:23350594-23350850 | Common:1; Rare:84 | ||||
| chr20:23361810-23362173 | Common:5; Rare:121 | ||||
| chr20:24992680-24992827 | Common:4; Rare:68 | ||||
| chr20:25195617-25195944 | Common:8; Rare:97 | ||||
| chr20:25247940-25248419 | Common:2; Rare:195 | ||||
| chr20:25290249-25290622 | Common:3; Rare:127 | ||||
| chr20:25293804-25294273 | Common:3; Rare:113 | ||||
| chr20:25300776-25301022 | Rare:79; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:25623956-25624140 | Common:1; Rare:60 | ||||
| chr20:25624414-25624600 | Common:2; Rare:48 | ||||
| chr20:25696766-25697091 | Common:3; Rare:92 | ||||
| chr20:31475246-31475304 | Rare:14 | ||||
| chr20:31547272-31547438 | Rare:45 | ||||
| chr20:31605090-31605577 | Common:11; Rare:266 | ||||
| chr20:31605580-31605983 | Common:2; Rare:204 |