| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:9760893-9761010 | Rare:15 | ||||
| chr12:9869352-9869568 | Common:3; Rare:36 | ||||
| chr12:10172043-10172248 | Rare:50 | ||||
| chr12:10212548-10212966 | Common:5; Rare:103 | ||||
| chr12:10307784-10307881 | Common:1; Rare:11 | ||||
| chr12:10613534-10613656 | Common:1; Rare:53 | ||||
| chr12:10721954-10722248 | Rare:68 | ||||
| chr12:10722840-10723008 | Common:2; Rare:56 | ||||
| chr12:10723134-10723459 | Common:5; Rare:103 | ||||
| chr12:11171163-11171228 | Rare:27 | ||||
| chr12:11171553-11171638 | Common:1; Rare:28 | ||||
| chr12:12357004-12357222 | Common:4; Rare:106 | ||||
| chr12:12560864-12561156 | Common:3; Rare:65 | ||||
| chr12:12611654-12612183 | Common:3; Rare:156 | ||||
| chr12:12717211-12717883 | Common:2; Rare:220; Clinvar:12; Clinvar (benign):9; Clinvar (pathogenic):1 |