| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51026321-51026515 | Common:3; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:51048077-51048379 | Common:2; Rare:107 | ||||
| chr12:51238648-51238914 | Common:8; Rare:115 | ||||
| chr12:51907328-51907615 | Rare:67; Clinvar:3 | ||||
| chr12:52006718-52006946 | Rare:44 | ||||
| chr12:52051118-52051493 | Common:1; Rare:123 | ||||
| chr12:52949826-52949965 | Rare:35 | ||||
| chr12:53006188-53006494 | Common:2; Rare:112 | ||||
| chr12:53046957-53047353 | Common:2; Rare:98 | ||||
| chr12:53048855-53049229 | Common:1; Rare:77 | ||||
| chr12:53049706-53050112 | Common:1; Rare:93 | ||||
| chr12:53063183-53063380 | Rare:56 | ||||
| chr12:53079344-53079559 | Common:2; Rare:74 | ||||
| chr12:53180470-53180719 | Common:2; Rare:95 | ||||
| chr12:53232172-53232432 | Common:2; Rare:55 |