| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107621-105107815 | Common:1; Rare:90; Clinvar:1 | ||||
| chr12:105236020-105236338 | Common:2; Rare:140 | ||||
| chr12:105330655-105330934 | Common:4; Rare:89 | ||||
| chr12:105331349-105331426 | Rare:13 | ||||
| chr12:106247371-106247545 | Common:2; Rare:44 | ||||
| chr12:106247919-106248141 | Common:1; Rare:67 | ||||
| chr12:106955623-106956063 | Common:3; Rare:152 | ||||
| chr12:106987035-106987310 | Common:5; Rare:77 | ||||
| chr12:107093514-107093661 | Rare:54 | ||||
| chr12:107685686-107685968 | Rare:89 | ||||
| chr12:108561013-108561481 | Common:6; Rare:139 | ||||
| chr12:108730400-108730645 | Common:1; Rare:64 | ||||
| chr12:109097846-109098221 | Common:5; Rare:119 | ||||
| chr12:109477229-109477634 | Common:3; Rare:106 | ||||
| chr12:109573483-109573826 | Common:3; Rare:98; Clinvar:3; Clinvar (benign):5 |