| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6598040-6598313 | Common:1; Rare:63 | ||||
| chr12:6606582-6606763 | Rare:67 | ||||
| chr12:6638984-6639312 | Common:2; Rare:65 | ||||
| chr12:6663063-6663274 | Rare:63 | ||||
| chr12:6688867-6689143 | Rare:85 | ||||
| chr12:6689293-6689760 | Common:3; Rare:131 | ||||
| chr12:6723828-6724316 | Common:2; Rare:108 | ||||
| chr12:6752922-6753205 | Common:6; Rare:88 | ||||
| chr12:6851227-6851417 | Rare:46 | ||||
| chr12:6851873-6852275 | Common:1; Rare:102 | ||||
| chr12:6867310-6867611 | Common:2; Rare:140; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6868069-6868161 | Common:4; Rare:37 | ||||
| chr12:6868915-6869169 | Rare:75; Clinvar:2 | ||||
| chr12:6873274-6873598 | Common:3; Rare:92 | ||||
| chr12:6904723-6905037 | Common:2; Rare:74 |