| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:62642293-62642505 | Common:3; Rare:78 | ||||
| chr20:62937370-62937545 | Common:3; Rare:55 | ||||
| chr20:62937829-62938165 | Common:2; Rare:120 | ||||
| chr20:62952561-62952800 | Common:4; Rare:64 | ||||
| chr20:63272493-63272858 | Common:6; Rare:100 | ||||
| chr20:63284218-63284330 | Rare:37 | ||||
| chr20:63520620-63520829 | Common:3; Rare:99 | ||||
| chr20:63574209-63574337 | Rare:31 | ||||
| chr20:63627020-63627282 | Rare:97 | ||||
| chr20:63653380-63653616 | Common:1; Rare:29 | ||||
| chr20:63658240-63658376 | Common:3; Rare:47 | ||||
| chr20:63707857-63708182 | Rare:99 | ||||
| chr20:63864917-63865334 | Common:2; Rare:144 | ||||
| chr20:63979450-63979604 | Rare:41 | ||||
| chr20:63980982-63981240 | Common:4; Rare:87; Clinvar:7; Clinvar (benign):4 |