| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38905526-38905712 | Common:3; Rare:52 | ||||
| chr12:38906737-38906813 | Common:1; Rare:15 | ||||
| chr12:39619785-39619954 | Common:1; Rare:29 | ||||
| chr12:40224811-40225108 | Common:5; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:42238164-42238483 | Common:1; Rare:106 | ||||
| chr12:42325956-42326242 | Common:2; Rare:91 | ||||
| chr12:43758745-43759031 | Common:2; Rare:78; Clinvar:2 | ||||
| chr12:43806237-43806385 | Common:2; Rare:52 | ||||
| chr12:45215976-45216247 | Common:1; Rare:80 | ||||
| chr12:45729559-45729996 | Common:1; Rare:142; Clinvar:1 | ||||
| chr12:45990382-45990961 | Common:3; Rare:187 | ||||
| chr12:45991973-45992083 | Common:2; Rare:31 | ||||
| chr12:46267310-46267492 | Rare:39 | ||||
| chr12:46268484-46268727 | Common:2; Rare:49 | ||||
| chr12:46268729-46269221 | Common:1; Rare:131 |