| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:75390880-75391109 | Common:1; Rare:70 | ||||
| chr12:75511578-75511851 | Rare:80 | ||||
| chr12:76031593-76031809 | Common:1; Rare:76 | ||||
| chr12:76084566-76084793 | Common:1; Rare:76 | ||||
| chr12:76348360-76348575 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76559815-76559924 | Rare:45 | ||||
| chr12:76764040-76764285 | Common:2; Rare:104 | ||||
| chr12:76878973-76879160 | Rare:63 | ||||
| chr12:78863726-78863993 | Rare:46 | ||||
| chr12:78864590-78865064 | Common:2; Rare:104 | ||||
| chr12:79690532-79690678 | Rare:42 | ||||
| chr12:79934907-79935288 | Common:1; Rare:150 | ||||
| chr12:79935307-79935355 | Rare:13 | ||||
| chr12:80937688-80937859 | Common:1; Rare:53 | ||||
| chr12:81077982-81078097 | Rare:29 |