| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21501556-21501915 | Common:4; Rare:95 | ||||
| chr12:21657754-21657908 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:21941220-21941293 | Rare:14 | ||||
| chr12:22334628-22335039 | Common:1; Rare:121 | ||||
| chr12:22544154-22544318 | Common:1; Rare:84 | ||||
| chr12:22544480-22544640 | Common:2; Rare:37 | ||||
| chr12:22625019-22625247 | Rare:117 | ||||
| chr12:25195114-25195344 | Common:2; Rare:64 | ||||
| chr12:26937936-26938056 | Common:3; Rare:37 | ||||
| chr12:26938267-26938528 | Common:3; Rare:98 | ||||
| chr12:27244023-27244328 | Common:2; Rare:98 | ||||
| chr12:27523995-27524287 | Rare:68 | ||||
| chr12:27710738-27710927 | Common:2; Rare:88 | ||||
| chr12:28190360-28190526 | Common:1; Rare:54 | ||||
| chr12:29381136-29381364 | Common:2; Rare:70 |