| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32273078-32273187 | Rare:10 | ||||
| chr12:32273840-32274075 | Common:6; Rare:70 | ||||
| chr12:32301247-32302430 | Common:19; Rare:237 | ||||
| chr12:32659300-32659580 | Rare:48 | ||||
| chr12:32681446-32681644 | Common:4; Rare:49 | ||||
| chr12:32754434-32754834 | Common:3; Rare:67 | ||||
| chr12:32754930-32755150 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
| chr12:38350857-38350959 | Rare:19 | ||||
| chr12:38614287-38614426 | Rare:35 | ||||
| chr12:38711144-38711345 | Common:1; Rare:44 | ||||
| chr12:38738587-38738808 | Common:3; Rare:41 | ||||
| chr12:38892378-38892858 | Common:2; Rare:110 | ||||
| chr12:38903246-38904221 | Common:8; Rare:266 | ||||
| chr12:38904952-38905086 | Rare:29 | ||||
| chr12:39441959-39442359 | Common:3; Rare:128 |