| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57006352-57006950 | Rare:184 | ||||
| chr12:57031070-57031769 | Common:2; Rare:152; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:57078605-57079232 | Common:12; Rare:395 | ||||
| chr12:57087639-57088290 | Common:5; Rare:347 | ||||
| chr12:57088490-57089320 | Common:6; Rare:701 | ||||
| chr12:57089234-57089900 | Common:7; Rare:265 | ||||
| chr12:57111173-57111515 | Common:4; Rare:124 | ||||
| chr12:57111720-57111984 | Common:3; Rare:118 | ||||
| chr12:57127590-57128110 | Common:2; Rare:173 | ||||
| chr12:57128268-57128383 | Rare:31 | ||||
| chr12:57128292-57128515 | Common:2; Rare:86 | ||||
| chr12:57216621-57216875 | Common:1; Rare:97 | ||||
| chr12:57229618-57229814 | Common:2; Rare:137 | ||||
| chr12:57229933-57230407 | Rare:226 | ||||
| chr12:57240490-57240747 | Rare:76 |