| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122526892-122527295 | Common:3; Rare:138 | ||||
| chr12:122980383-122980743 | Common:1; Rare:123 | ||||
| chr12:123233096-123233512 | Common:2; Rare:141; Clinvar:1 | ||||
| chr12:123364825-123364948 | Common:1; Rare:46 | ||||
| chr12:123584393-123584604 | Common:2; Rare:78 | ||||
| chr12:123601834-123602184 | Common:6; Rare:100 | ||||
| chr12:123633624-123633868 | Common:2; Rare:116; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:130871761-130872116 | Common:4; Rare:143 | ||||
| chr12:131710795-131711107 | Rare:82 | ||||
| chr12:132084127-132084323 | Common:4; Rare:71 | ||||
| chr12:132956276-132956363 | Common:1; Rare:21 | ||||
| chr12:133037232-133037533 | Common:4; Rare:62 | ||||
| chr12:133130232-133130611 | Common:7; Rare:117 | ||||
| chr13:20773941-20774018 | Rare:24 | ||||
| chr13:21176508-21176717 | Common:1; Rare:100 |