| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:10716821-10716973 | Common:1; Rare:28 | ||||
| chr12:12808071-12808206 | Common:1; Rare:17 | ||||
| chr12:26126137-26126204 | Rare:19 | ||||
| chr12:45244594-45244787 | Rare:36 | ||||
| chr12:45302083-45302302 | Common:2; Rare:46; Clinvar (benign):1 | ||||
| chr12:45727464-45727592 | Rare:65 | ||||
| chr12:46383575-46383712 | Common:2; Rare:29 | ||||
| chr12:46387859-46387900 | Rare:3 | ||||
| chr12:46779951-46780152 | Common:1; Rare:39 | ||||
| chr12:49060769-49060903 | Common:1; Rare:51 | ||||
| chr12:51218308-51218359 | Common:1; Rare:11 | ||||
| chr12:51218363-51218464 | Rare:17 | ||||
| chr12:52032930-52032978 | Common:1; Rare:14 | ||||
| chr12:53052573-53052838 | Rare:42 | ||||
| chr12:55703378-55703674 | Common:1; Rare:36 |