| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:9072357-9072802 | Rare:102 | ||||
| chr12:9077335-9077642 | Common:3; Rare:66 | ||||
| chr12:9093508-9093734 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr12:9095617-9095893 | Common:3; Rare:72 | ||||
| chr12:9104211-9104496 | Common:1; Rare:73 | ||||
| chr12:9107527-9107741 | Common:4; Rare:47 | ||||
| chr12:9109124-9109130 | |||||
| chr12:10716928-10717173 | Rare:31 | ||||
| chr12:24562337-24562493 | Common:1; Rare:38 | ||||
| chr12:47789557-47789817 | Rare:49 | ||||
| chr12:49060746-49060844 | Common:1; Rare:48 | ||||
| chr12:52007813-52008110 | Common:1; Rare:59 | ||||
| chr12:53067649-53067773 | Common:1; Rare:29 | ||||
| chr12:54415637-54415880 | Common:2; Rare:31 | ||||
| chr12:55697193-55697477 | Common:3; Rare:78; Clinvar (benign):6 |