| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6493778-6494146 | Common:2; Rare:109 | ||||
| chr12:6536403-6536788 | Rare:132 | ||||
| chr12:6549108-6549258 | Common:1; Rare:25 | ||||
| chr12:6568234-6568384 | Rare:58 | ||||
| chr12:6606411-6606605 | Common:3; Rare:71 | ||||
| chr12:6663091-6663403 | Common:2; Rare:89 | ||||
| chr12:6688897-6689089 | Rare:63 | ||||
| chr12:6723963-6724306 | Common:1; Rare:86 | ||||
| chr12:6752947-6753189 | Common:6; Rare:77 | ||||
| chr12:6851227-6851486 | Rare:62 | ||||
| chr12:6851922-6852174 | Rare:63 | ||||
| chr12:6867365-6867594 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873330-6873532 | Common:1; Rare:57 | ||||
| chr12:6943531-6943818 | Common:4; Rare:117 | ||||
| chr12:6943928-6944165 | Common:7; Rare:238; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 |