| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12357023-12357098 | Common:1; Rare:38 | ||||
| chr12:14771124-14771241 | Rare:37 | ||||
| chr12:14803449-14803680 | Common:1; Rare:56 | ||||
| chr12:15882319-15882609 | Common:1; Rare:77 | ||||
| chr12:21501556-21501828 | Common:2; Rare:67 | ||||
| chr12:24949008-24949192 | Common:1; Rare:49 | ||||
| chr12:26938276-26938522 | Common:1; Rare:92 | ||||
| chr12:27523990-27524206 | Rare:54 | ||||
| chr12:30754867-30755082 | Rare:94 | ||||
| chr12:31073755-31073892 | Common:7; Rare:54 | ||||
| chr12:31074100-31074250 | Common:1; Rare:29 | ||||
| chr12:31729012-31729290 | Common:1; Rare:83 | ||||
| chr12:31959271-31959483 | Common:2; Rare:68 | ||||
| chr12:32755248-32755366 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:42326023-42326206 | Common:1; Rare:60 |