| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49812767-49812925 | Common:2; Rare:43 | ||||
| chr20:49915491-49915567 | Common:2; Rare:25 | ||||
| chr20:50113112-50113239 | Common:5; Rare:61 | ||||
| chr20:50115921-50116080 | Common:1; Rare:39 | ||||
| chr20:50903906-50904169 | Rare:64 | ||||
| chr20:50958481-50958851 | Common:1; Rare:130; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:52972665-52972841 | Common:2; Rare:41 | ||||
| chr20:53593783-53593914 | Common:1; Rare:50 | ||||
| chr20:54173982-54174112 | Rare:37 | ||||
| chr20:56392138-56392703 | Common:6; Rare:151 | ||||
| chr20:56468559-56468700 | Rare:65 | ||||
| chr20:57266594-57266781 | Common:1; Rare:55 | ||||
| chr20:57710065-57710269 | Common:1; Rare:57 | ||||
| chr20:58389035-58389321 | Common:4; Rare:155; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:58515390-58515534 | Common:2; Rare:26 |