| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:25195155-25195308 | Common:1; Rare:48 | ||||
| chr12:26937936-26938067 | Common:3; Rare:39 | ||||
| chr12:26938263-26938534 | Common:3; Rare:103 | ||||
| chr12:27244038-27244315 | Common:2; Rare:87 | ||||
| chr12:27332764-27332995 | Common:2; Rare:77 | ||||
| chr12:27523990-27524287 | Rare:69 | ||||
| chr12:27710690-27710887 | Common:2; Rare:82 | ||||
| chr12:28190330-28190500 | Common:2; Rare:63 | ||||
| chr12:29381139-29381387 | Common:3; Rare:76 | ||||
| chr12:30695853-30696007 | Common:1; Rare:35 | ||||
| chr12:30754758-30755051 | Common:1; Rare:115 | ||||
| chr12:31073743-31073892 | Common:7; Rare:58 | ||||
| chr12:31728996-31729267 | Rare:81 | ||||
| chr12:31959325-31959482 | Common:1; Rare:50 | ||||
| chr12:32679128-32679350 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):3 |