| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:21501532-21501891 | Common:3; Rare:98 | ||||
| chr12:21657754-21657996 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:22625019-22625235 | Rare:112 | ||||
| chr12:24948986-24949329 | Common:4; Rare:73 | ||||
| chr12:25195151-25195308 | Common:1; Rare:48 | ||||
| chr12:25959321-25959382 | Common:1; Rare:15 | ||||
| chr12:26937936-26938056 | Common:3; Rare:37 | ||||
| chr12:26938259-26938552 | Common:3; Rare:110 | ||||
| chr12:27332705-27333016 | Common:2; Rare:101 | ||||
| chr12:27523990-27524303 | Rare:72 | ||||
| chr12:27710738-27710887 | Common:2; Rare:67 | ||||
| chr12:28190372-28190506 | Common:1; Rare:41 | ||||
| chr12:29149019-29149323 | Rare:88 | ||||
| chr12:30695860-30696019 | Common:1; Rare:36 | ||||
| chr12:30754762-30755138 | Common:3; Rare:142 |