| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:30695846-30695977 | Common:1; Rare:36 | ||||
| chr12:30754740-30755088 | Common:1; Rare:136 | ||||
| chr12:31073716-31073884 | Common:7; Rare:58 | ||||
| chr12:31326103-31326299 | Common:3; Rare:67 | ||||
| chr12:31728993-31729229 | Rare:73 | ||||
| chr12:31959282-31959488 | Common:2; Rare:65 | ||||
| chr12:32501936-32502286 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:32679086-32679358 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:32755420-32755529 | Rare:41; Clinvar (pathogenic):1 | ||||
| chr12:32755867-32755991 | Rare:48 | ||||
| chr12:32896764-32896999 | Common:3; Rare:78; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:33439758-33440080 | Common:2; Rare:106 | ||||
| chr12:38905526-38905787 | Common:5; Rare:71 | ||||
| chr12:38906287-38906411 | Common:1; Rare:31 | ||||
| chr12:39442841-39443071 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):2 |