| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93571738-93571890 | Common:6; Rare:57 | ||||
| chr12:94459833-94460064 | Common:2; Rare:69 | ||||
| chr12:95003605-95003814 | Common:3; Rare:88; Clinvar (benign):6 | ||||
| chr12:95217377-95217769 | Common:4; Rare:106 | ||||
| chr12:95474006-95474210 | Common:2; Rare:97 | ||||
| chr12:96907147-96907298 | Common:1; Rare:57 | ||||
| chr12:98644697-98644859 | Common:3; Rare:54 | ||||
| chr12:98645073-98645317 | Common:2; Rare:68 | ||||
| chr12:100267060-100267279 | Common:1; Rare:105 | ||||
| chr12:101407668-101408037 | Common:3; Rare:90 | ||||
| chr12:102120048-102120223 | Rare:68 | ||||
| chr12:103930098-103930536 | Common:8; Rare:150 | ||||
| chr12:103957122-103957335 | Common:6; Rare:62 | ||||
| chr12:103965698-103965947 | Common:2; Rare:59 | ||||
| chr12:104064159-104064298 | Common:1; Rare:26 |