| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:19977129-19977357 | Common:1; Rare:53 | ||||
| chr20:19992987-19993274 | Common:3; Rare:42 | ||||
| chr20:20024451-20024694 | Common:1; Rare:40 | ||||
| chr20:20030125-20030407 | Common:1; Rare:34 | ||||
| chr20:20031394-20031706 | Common:2; Rare:44 | ||||
| chr20:20032171-20032653 | Common:2; Rare:134 | ||||
| chr20:20033749-20033901 | Common:3; Rare:25 | ||||
| chr20:20486767-20486906 | Common:1; Rare:24 | ||||
| chr20:20606560-20606609 | Rare:4 | ||||
| chr20:20638988-20639255 | Common:2; Rare:38 | ||||
| chr20:20679653-20679766 | Common:1; Rare:18 | ||||
| chr20:21166303-21166612 | Common:4; Rare:66 | ||||
| chr20:21330522-21330706 | Rare:50 | ||||
| chr20:21333703-21334185 | Common:1; Rare:115 | ||||
| chr20:23047402-23047507 | Common:3; Rare:28; Clinvar (benign):5 |