| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132084085-132084338 | Common:6; Rare:94 | ||||
| chr12:132144109-132144491 | Common:2; Rare:133 | ||||
| chr12:132286363-132286884 | Common:4; Rare:128 | ||||
| chr12:132687313-132687696 | Common:4; Rare:142; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132829064-132829239 | Rare:83 | ||||
| chr12:132887553-132887842 | Rare:85 | ||||
| chr12:132956254-132956422 | Common:1; Rare:37 | ||||
| chr12:132986230-132986448 | Rare:53 | ||||
| chr12:133080143-133080454 | Common:7; Rare:99 | ||||
| chr12:133130238-133130712 | Common:7; Rare:155 | ||||
| chr13:19633355-19633774 | Common:1; Rare:153 | ||||
| chr13:19782923-19783082 | Common:2; Rare:58 | ||||
| chr13:19863448-19863866 | Common:5; Rare:145 | ||||
| chr13:20525778-20525977 | Common:1; Rare:74 | ||||
| chr13:21061522-21061722 | Common:1; Rare:63 |