| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:93677219-93677703 | Common:1; Rare:199 | ||||
| chr12:93677759-93677984 | Common:1; Rare:39 | ||||
| chr12:94148230-94148870 | Common:1; Rare:131 | ||||
| chr12:94331670-94332070 | Rare:70; Clinvar (benign):1 | ||||
| chr12:94459768-94460162 | Common:9; Rare:262 | ||||
| chr12:94460369-94460769 | Rare:95 | ||||
| chr12:94615360-94615950 | Common:3; Rare:98 | ||||
| chr12:94650450-94650820 | Common:4; Rare:168 | ||||
| chr12:95003566-95003902 | Common:10; Rare:274; Clinvar (benign):12 | ||||
| chr12:95072945-95073217 | Common:6; Rare:184 | ||||
| chr12:95073413-95073683 | Common:3; Rare:159 | ||||
| chr12:95217331-95217922 | Common:16; Rare:431 | ||||
| chr12:95218015-95218327 | Common:6; Rare:117 | ||||
| chr12:95473847-95474274 | Common:7; Rare:379 | ||||
| chr12:95858783-95859115 | Common:6; Rare:167 |