| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:27332776-27333067 | Common:3; Rare:100 | ||||
| chr12:27523990-27524249 | Rare:62 | ||||
| chr12:28190378-28190483 | Common:1; Rare:30 | ||||
| chr12:30754764-30755078 | Common:1; Rare:128 | ||||
| chr12:31073784-31073886 | Rare:40 | ||||
| chr12:31729012-31729302 | Common:1; Rare:92 | ||||
| chr12:31959240-31959488 | Common:2; Rare:80 | ||||
| chr12:32896757-32896981 | Common:1; Rare:75; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905573-38905671 | Common:3; Rare:26 | ||||
| chr12:42326031-42326176 | Common:1; Rare:50 | ||||
| chr12:43758753-43758996 | Common:2; Rare:68; Clinvar:2 | ||||
| chr12:43806241-43806385 | Common:2; Rare:50 | ||||
| chr12:45215982-45216163 | Common:1; Rare:61 | ||||
| chr12:45729626-45729821 | Rare:55 | ||||
| chr12:45990482-45990959 | Common:2; Rare:155 |