| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93441864-93442006 | Common:1; Rare:50 | ||||
| chr12:93442046-93442186 | Rare:35 | ||||
| chr12:93571709-93571912 | Common:7; Rare:79 | ||||
| chr12:94459815-94459992 | Common:3; Rare:47 | ||||
| chr12:95003593-95003821 | Common:3; Rare:95; Clinvar (benign):6 | ||||
| chr12:95217377-95217840 | Common:4; Rare:125 | ||||
| chr12:95474039-95474285 | Common:2; Rare:110 | ||||
| chr12:95858822-95859033 | Common:2; Rare:57 | ||||
| chr12:98515811-98516069 | Rare:98; Clinvar:6; Clinvar (benign):4 | ||||
| chr12:98644703-98644843 | Common:3; Rare:47 | ||||
| chr12:98644986-98645317 | Common:2; Rare:98 | ||||
| chr12:100267047-100267312 | Common:1; Rare:119 | ||||
| chr12:100573545-100573761 | Rare:73 | ||||
| chr12:101280029-101280172 | Common:1; Rare:43 | ||||
| chr12:101407641-101408035 | Common:3; Rare:97 |