| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:62796292-62796512 | Rare:79 | ||||
| chr20:62861764-62862073 | Common:12; Rare:99 | ||||
| chr20:62926270-62926720 | Common:3; Rare:138 | ||||
| chr20:62937381-62937489 | Common:2; Rare:33 | ||||
| chr20:62937820-62938062 | Common:1; Rare:79 | ||||
| chr20:63216091-63216432 | Common:2; Rare:124 | ||||
| chr20:63253439-63253694 | Common:3; Rare:75 | ||||
| chr20:63254433-63254715 | Common:1; Rare:97 | ||||
| chr20:63272645-63272837 | Common:5; Rare:62 | ||||
| chr20:63377340-63377840 | Common:5; Rare:124 | ||||
| chr20:63472019-63472222 | Common:3; Rare:50; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:63499077-63499251 | Common:1; Rare:38 | ||||
| chr20:63520121-63520300 | Common:1; Rare:40 | ||||
| chr20:63520602-63520810 | Common:5; Rare:98 | ||||
| chr20:63521067-63521287 | Common:5; Rare:54 |