| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:133080523-133081136 | Common:4; Rare:176 | ||||
| chr12:133081143-133081268 | Rare:36 | ||||
| chr12:133130190-133130720 | Common:7; Rare:179 | ||||
| chr12:133181337-133181609 | Common:2; Rare:83 | ||||
| chr12:133181889-133181917 | Rare:4 | ||||
| chr13:19633311-19633763 | Common:1; Rare:160 | ||||
| chr13:19782884-19783130 | Common:2; Rare:90 | ||||
| chr13:19863358-19863972 | Common:6; Rare:219 | ||||
| chr13:19864052-19864344 | Common:1; Rare:85 | ||||
| chr13:19958383-19958766 | Common:5; Rare:165 | ||||
| chr13:19958880-19959074 | Common:2; Rare:68 | ||||
| chr13:19959412-19959499 | Common:1; Rare:32 | ||||
| chr13:19960215-19960289 | Rare:22 | ||||
| chr13:20160948-20161260 | Common:3; Rare:104; Clinvar (benign):1 | ||||
| chr13:20161275-20161466 | Common:1; Rare:48 |