| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94459798-94460047 | Common:3; Rare:70 | ||||
| chr12:95217384-95217769 | Common:4; Rare:105 | ||||
| chr12:95473976-95474203 | Common:2; Rare:101 | ||||
| chr12:95548796-95548903 | Common:2; Rare:40 | ||||
| chr12:95858817-95859033 | Common:2; Rare:60 | ||||
| chr12:96489450-96489598 | Common:2; Rare:34 | ||||
| chr12:96907195-96907295 | Rare:40 | ||||
| chr12:98515503-98515960 | Rare:155; Clinvar:8; Clinvar (benign):2 | ||||
| chr12:98644944-98645296 | Common:2; Rare:104 | ||||
| chr12:100200717-100200851 | Rare:44 | ||||
| chr12:100267047-100267277 | Common:1; Rare:112 | ||||
| chr12:101407641-101408025 | Common:3; Rare:92 | ||||
| chr12:102120060-102120229 | Rare:66 | ||||
| chr12:103930014-103930554 | Common:9; Rare:180 | ||||
| chr12:103965674-103965941 | Common:2; Rare:71 |