| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7130221-7130371 | Common:5; Rare:39 | ||||
| chr12:7189551-7189731 | Rare:66; Clinvar:4 | ||||
| chr12:8032590-8032773 | Rare:65 | ||||
| chr12:8066316-8066390 | Rare:14 | ||||
| chr12:8227584-8227691 | Rare:28 | ||||
| chr12:8823236-8823882 | Common:2; Rare:187; Clinvar:3; Clinvar (benign):7 | ||||
| chr12:8914397-8914763 | Common:6; Rare:113 | ||||
| chr12:8949589-8949865 | Common:1; Rare:56 | ||||
| chr12:8949941-8950073 | Common:1; Rare:36 | ||||
| chr12:9115762-9116038 | Common:3; Rare:69 | ||||
| chr12:9116114-9116268 | Rare:36 | ||||
| chr12:9607908-9608047 | Common:1; Rare:24 | ||||
| chr12:9869330-9869625 | Common:3; Rare:48 | ||||
| chr12:10390032-10390153 | Rare:25 | ||||
| chr12:10613491-10613732 | Common:1; Rare:94 |