| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:24902085-24902325 | Common:1; Rare:51 | ||||
| chr12:25195142-25195308 | Common:1; Rare:50 | ||||
| chr12:26937932-26938179 | Common:8; Rare:69 | ||||
| chr12:26938263-26938527 | Common:3; Rare:99 | ||||
| chr12:27523990-27524317 | Rare:74 | ||||
| chr12:28190404-28190502 | Common:1; Rare:33 | ||||
| chr12:30695860-30696011 | Common:1; Rare:33 | ||||
| chr12:31073760-31073872 | Common:6; Rare:42 | ||||
| chr12:31324080-31324312 | Rare:53 | ||||
| chr12:31326179-31326522 | Common:4; Rare:108 | ||||
| chr12:31729015-31729270 | Rare:76 | ||||
| chr12:31959262-31959488 | Common:2; Rare:73 | ||||
| chr12:32679050-32679343 | Common:2; Rare:111; Clinvar (benign):3 | ||||
| chr12:32755225-32755330 | Common:1; Rare:30; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr12:38905560-38905712 | Common:3; Rare:40 |