| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120201081-120201354 | Common:2; Rare:88 | ||||
| chr12:120437842-120438198 | Common:2; Rare:131; Clinvar (benign):2 | ||||
| chr12:120446322-120446495 | Common:2; Rare:77 | ||||
| chr12:120469484-120469895 | Common:5; Rare:139 | ||||
| chr12:120495845-120496228 | Common:7; Rare:128 | ||||
| chr12:120581358-120581564 | Common:1; Rare:75 | ||||
| chr12:121399947-121400171 | Common:2; Rare:83 | ||||
| chr12:121580244-121580430 | Rare:65 | ||||
| chr12:121580997-121581078 | Rare:9 | ||||
| chr12:121672599-121672699 | Common:4; Rare:34 | ||||
| chr12:121802940-121803086 | Rare:35 | ||||
| chr12:121888651-121888868 | Common:2; Rare:68 | ||||
| chr12:122526864-122527291 | Common:4; Rare:152 | ||||
| chr12:122974566-122974767 | Rare:51 | ||||
| chr12:122975151-122975254 | Common:1; Rare:33 |