| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:88580440-88580541 | Common:1; Rare:36 | ||||
| chr12:89352495-89352711 | Rare:61 | ||||
| chr12:89525375-89525621 | Common:1; Rare:58 | ||||
| chr12:89709314-89709484 | Common:1; Rare:70 | ||||
| chr12:93677243-93677399 | Rare:35 | ||||
| chr12:94459833-94460020 | Common:2; Rare:53 | ||||
| chr12:95217431-95217746 | Common:3; Rare:85 | ||||
| chr12:98515428-98515675 | Rare:85; Clinvar:1 | ||||
| chr12:98593447-98593747 | Common:2; Rare:103; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:98644720-98645293 | Common:6; Rare:165 | ||||
| chr12:100200717-100200834 | Rare:37 | ||||
| chr12:100573561-100573740 | Rare:62 | ||||
| chr12:101407692-101408056 | Common:3; Rare:86 | ||||
| chr12:102120062-102120262 | Rare:80 | ||||
| chr12:103930345-103930529 | Common:4; Rare:85 |