| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:24931869-24932319 | Common:3; Rare:96 | ||||
| chr20:24932451-24932613 | Rare:32 | ||||
| chr20:25292201-25292515 | Common:5; Rare:118; Clinvar (pathogenic):1 | ||||
| chr20:25532852-25532996 | Common:2; Rare:23 | ||||
| chr20:25751081-25751223 | Rare:34 | ||||
| chr20:25853988-25854118 | Common:3; Rare:48 | ||||
| chr20:29080162-29080249 | |||||
| chr20:30580060-30580251 | Common:1; Rare:35 | ||||
| chr20:31572894-31573010 | Rare:27 | ||||
| chr20:31604221-31604458 | Common:1; Rare:97 | ||||
| chr20:31605830-31606190 | Common:2; Rare:177 | ||||
| chr20:31608576-31608802 | Rare:74 | ||||
| chr20:31674824-31675118 | Common:1; Rare:45 | ||||
| chr20:32453463-32453633 | Common:1; Rare:49 | ||||
| chr20:32537167-32537310 | Rare:27 |