| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31958907-31959202 | Common:2; Rare:65 | ||||
| chr12:31959282-31959488 | Common:2; Rare:65 | ||||
| chr12:32755456-32755717 | Common:1; Rare:88; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr12:32755870-32755997 | Rare:47 | ||||
| chr12:32896744-32896999 | Common:4; Rare:83; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:38905532-38905752 | Common:4; Rare:59 | ||||
| chr12:39619804-39619919 | Common:1; Rare:21 | ||||
| chr12:40224957-40225060 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chr12:42325939-42326228 | Common:1; Rare:91 | ||||
| chr12:43758749-43759061 | Common:2; Rare:84; Clinvar:2 | ||||
| chr12:43806090-43806379 | Common:4; Rare:111 | ||||
| chr12:45215978-45216174 | Common:1; Rare:64 | ||||
| chr12:45990425-45990894 | Common:2; Rare:146 | ||||
| chr12:46268479-46268825 | Common:2; Rare:80 | ||||
| chr12:46269654-46269673 | Rare:2 |