| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49758223-49758410 | Common:3; Rare:57 | ||||
| chr12:49759142-49759321 | Rare:54 | ||||
| chr12:49828362-49828595 | Common:1; Rare:88 | ||||
| chr12:49843092-49843254 | Common:1; Rare:48 | ||||
| chr12:49903856-49904229 | Common:3; Rare:89 | ||||
| chr12:50085064-50085389 | Common:1; Rare:89 | ||||
| chr12:50167284-50167597 | Common:3; Rare:96 | ||||
| chr12:50283420-50283672 | Common:3; Rare:74 | ||||
| chr12:50400780-50401035 | Common:1; Rare:83 | ||||
| chr12:50763931-50764326 | Common:1; Rare:104 | ||||
| chr12:51026313-51026495 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048074-51048376 | Common:2; Rare:107 | ||||
| chr12:51173027-51173185 | Rare:30 | ||||
| chr12:51238647-51238914 | Common:8; Rare:115 | ||||
| chr12:51270165-51270288 | Common:1; Rare:29 |