| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:92145825-92146209 | Common:2; Rare:121 | ||||
| chr12:92929293-92929521 | Rare:62 | ||||
| chr12:93377709-93377966 | Rare:89 | ||||
| chr12:93441866-93442168 | Common:2; Rare:96 | ||||
| chr12:93677312-93677390 | Rare:16 | ||||
| chr12:94459823-94460003 | Common:2; Rare:48 | ||||
| chr12:95217290-95217769 | Common:6; Rare:128 | ||||
| chr12:95473867-95474255 | Common:3; Rare:154 | ||||
| chr12:95548784-95548931 | Common:3; Rare:49 | ||||
| chr12:95551308-95551680 | Common:4; Rare:74 | ||||
| chr12:95858822-95859076 | Common:3; Rare:74 | ||||
| chr12:98515428-98515823 | Rare:136; Clinvar:5 | ||||
| chr12:98515832-98515927 | Rare:34; Clinvar (benign):1 | ||||
| chr12:98515929-98515947 | Rare:4; Clinvar:2 | ||||
| chr12:98593474-98593783 | Common:2; Rare:101; Clinvar:4; Clinvar (benign):4 |