| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35616841-35617072 | Common:1; Rare:42 | ||||
| chr20:35664880-35665045 | Common:1; Rare:42 | ||||
| chr20:35699190-35699279 | Rare:14 | ||||
| chr20:35699295-35699481 | Rare:66; Clinvar (benign):3 | ||||
| chr20:35740823-35741128 | Common:3; Rare:83 | ||||
| chr20:35741622-35741699 | Common:1; Rare:25 | ||||
| chr20:35742165-35742685 | Common:6; Rare:171 | ||||
| chr20:35771793-35772050 | Common:2; Rare:80 | ||||
| chr20:36236389-36236543 | Common:1; Rare:40 | ||||
| chr20:36461144-36461502 | Common:1; Rare:105 | ||||
| chr20:36472876-36473087 | Common:1; Rare:33 | ||||
| chr20:36541362-36541579 | Common:3; Rare:59 | ||||
| chr20:36573295-36573637 | Common:1; Rare:146 | ||||
| chr20:36574381-36574567 | Rare:69 | ||||
| chr20:36746062-36746291 | Common:2; Rare:84 |