| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7189620-7189731 | Rare:46; Clinvar:4 | ||||
| chr12:8033465-8033594 | Rare:35 | ||||
| chr12:8227599-8227691 | Rare:26 | ||||
| chr12:8914374-8914735 | Common:6; Rare:106 | ||||
| chr12:8949601-8949983 | Common:4; Rare:83 | ||||
| chr12:10613540-10613635 | Rare:39 | ||||
| chr12:10673986-10674162 | Common:1; Rare:34 | ||||
| chr12:11171158-11171250 | Common:1; Rare:37 | ||||
| chr12:11171551-11171642 | Common:2; Rare:30 | ||||
| chr12:12356999-12357196 | Common:4; Rare:104 | ||||
| chr12:12560898-12561156 | Common:3; Rare:53 | ||||
| chr12:12562244-12562575 | Common:3; Rare:82 | ||||
| chr12:12891314-12891575 | Common:1; Rare:50 | ||||
| chr12:13000196-13000476 | Common:2; Rare:90 | ||||
| chr12:13103631-13103715 | Rare:21 |