| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12357027-12357150 | Common:2; Rare:65 | ||||
| chr12:14803455-14803670 | Common:1; Rare:51 | ||||
| chr12:21501565-21501831 | Common:1; Rare:63 | ||||
| chr12:26938257-26938541 | Common:3; Rare:107 | ||||
| chr12:31959290-31959470 | Common:2; Rare:56 | ||||
| chr12:32399355-32399567 | Common:2; Rare:50 | ||||
| chr12:32755464-32755590 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:38905588-38905684 | Common:3; Rare:27 | ||||
| chr12:42326084-42326205 | Common:1; Rare:33 | ||||
| chr12:43758757-43758997 | Common:2; Rare:67; Clinvar:2 | ||||
| chr12:45215989-45216158 | Common:1; Rare:55 | ||||
| chr12:47705970-47706116 | Rare:64 | ||||
| chr12:48815436-48815600 | Common:1; Rare:40 | ||||
| chr12:49018741-49019082 | Common:1; Rare:114; Clinvar (benign):1 | ||||
| chr12:49131334-49131614 | Common:2; Rare:109 |