| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:89708796-89709099 | Common:1; Rare:116 | ||||
| chr12:91111398-91111553 | Common:3; Rare:42 | ||||
| chr12:92145837-92146121 | Common:2; Rare:87 | ||||
| chr12:92929248-92929521 | Common:1; Rare:85 | ||||
| chr12:93377722-93377966 | Rare:83 | ||||
| chr12:93441880-93442147 | Common:2; Rare:86 | ||||
| chr12:93570881-93571075 | Rare:52 | ||||
| chr12:93571734-93571912 | Common:7; Rare:67 | ||||
| chr12:93572360-93572704 | Common:1; Rare:81 | ||||
| chr12:93677262-93677390 | Rare:26 | ||||
| chr12:94459820-94460053 | Common:2; Rare:68 | ||||
| chr12:95003660-95003789 | Common:3; Rare:51; Clinvar (benign):3 | ||||
| chr12:95217357-95217884 | Common:6; Rare:142 | ||||
| chr12:95473997-95474225 | Common:2; Rare:109 | ||||
| chr12:95548788-95548922 | Common:2; Rare:46 |