| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:130954185-130954342 | Common:1; Rare:27 | ||||
| chr12:131710795-131711113 | Rare:84 | ||||
| chr12:131929018-131929295 | Common:10; Rare:84; Clinvar:1 | ||||
| chr12:132084087-132084331 | Common:6; Rare:90 | ||||
| chr12:132144109-132144491 | Common:2; Rare:133 | ||||
| chr12:132687298-132687683 | Common:4; Rare:143; Clinvar:9; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710557-132711042 | Common:5; Rare:156 | ||||
| chr12:132829048-132829241 | Rare:88 | ||||
| chr12:132887552-132887810 | Rare:79 | ||||
| chr12:132956242-132956422 | Common:1; Rare:40 | ||||
| chr12:133037209-133037536 | Common:4; Rare:66 | ||||
| chr12:133130232-133130652 | Common:7; Rare:139 | ||||
| chr13:19659040-19659275 | Rare:66 | ||||
| chr13:19863445-19863927 | Common:6; Rare:176 | ||||
| chr13:20525796-20525962 | Common:1; Rare:65 |