| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46778601-46778898 | Common:1; Rare:65 | ||||
| chr12:46779609-46779764 | Rare:39 | ||||
| chr12:46788525-46788822 | Common:6; Rare:66 | ||||
| chr12:46938357-46938565 | Common:3; Rare:27 | ||||
| chr12:49060774-49060902 | Common:1; Rare:49 | ||||
| chr12:52076701-52076866 | Common:1; Rare:42 | ||||
| chr12:53027781-53028182 | Common:1; Rare:138 | ||||
| chr12:53051582-53051721 | Rare:22 | ||||
| chr12:53443255-53443579 | Common:2; Rare:91 | ||||
| chr12:55685216-55685413 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:55686661-55686749 | Rare:19 | ||||
| chr12:55688019-55688270 | Common:2; Rare:85; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:55981041-55981129 | Rare:22 | ||||
| chr12:56165689-56165714 | Rare:5 | ||||
| chr12:56634989-56635116 | Rare:22 |