| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93377746-93377956 | Rare:65 | ||||
| chr12:93441876-93442141 | Common:2; Rare:86 | ||||
| chr12:93571766-93571902 | Common:6; Rare:56 | ||||
| chr12:94459811-94460043 | Common:3; Rare:64 | ||||
| chr12:95003627-95003777 | Common:3; Rare:63; Clinvar (benign):4 | ||||
| chr12:95217365-95217784 | Common:5; Rare:117 | ||||
| chr12:95473903-95474252 | Common:3; Rare:146 | ||||
| chr12:95996163-95996506 | Common:3; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:96399356-96399656 | Common:2; Rare:87 | ||||
| chr12:96400104-96400361 | Common:2; Rare:71 | ||||
| chr12:96907174-96907293 | Rare:42 | ||||
| chr12:98515494-98515653 | Rare:47; Clinvar:1 | ||||
| chr12:98515820-98515886 | Rare:29; Clinvar (benign):1 | ||||
| chr12:98645104-98645317 | Common:1; Rare:62 | ||||
| chr12:100200707-100200846 | Rare:43 |