| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31728995-31729301 | Common:1; Rare:98 | ||||
| chr12:31959323-31959488 | Common:1; Rare:53 | ||||
| chr12:32679086-32679332 | Common:1; Rare:91; Clinvar (benign):1 | ||||
| chr12:32896744-32896981 | Common:2; Rare:77; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:38905526-38905813 | Common:6; Rare:83 | ||||
| chr12:39619722-39620112 | Common:2; Rare:61 | ||||
| chr12:40224901-40225116 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:42238164-42238445 | Common:1; Rare:87 | ||||
| chr12:42326011-42326226 | Common:1; Rare:71 | ||||
| chr12:43758749-43758996 | Common:2; Rare:68; Clinvar:2 | ||||
| chr12:43806241-43806407 | Common:2; Rare:55 | ||||
| chr12:45215978-45216212 | Common:1; Rare:75 | ||||
| chr12:45990382-45990667 | Common:1; Rare:94 | ||||
| chr12:46362284-46362523 | Common:2; Rare:61 | ||||
| chr12:46371300-46371432 | Common:1; Rare:53 |