| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123972946-123973303 | Common:2; Rare:110 | ||||
| chr12:124989071-124989307 | Common:4; Rare:64 | ||||
| chr12:130716247-130716392 | Rare:20 | ||||
| chr12:130839160-130839386 | Common:2; Rare:82 | ||||
| chr12:130871723-130872126 | Common:4; Rare:168 | ||||
| chr12:131710795-131711110 | Rare:83 | ||||
| chr12:132687329-132687685 | Common:4; Rare:128; Clinvar:2; Clinvar (benign):7 | ||||
| chr12:132887553-132887841 | Rare:85 | ||||
| chr12:132956271-132956437 | Common:1; Rare:35 | ||||
| chr12:132986196-132986464 | Rare:68 | ||||
| chr12:133037201-133037536 | Common:5; Rare:67 | ||||
| chr12:133080724-133080954 | Rare:71 | ||||
| chr12:133130249-133130659 | Common:7; Rare:139 | ||||
| chr13:20525796-20525941 | Common:1; Rare:60 | ||||
| chr13:20773937-20774018 | Rare:27 |