| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25041917-25042295 | Common:4; Rare:99 | ||||
| chr2:25342454-25342789 | Common:1; Rare:72 | ||||
| chr2:25673401-25673740 | Common:1; Rare:117 | ||||
| chr2:25878407-25878781 | Common:5; Rare:112 | ||||
| chr2:26033741-26034194 | Common:4; Rare:171 | ||||
| chr2:26034202-26034428 | Common:2; Rare:67 | ||||
| chr2:26242773-26242875 | Common:4; Rare:21 | ||||
| chr2:26243049-26243268 | Common:1; Rare:37 | ||||
| chr2:26244573-26244990 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345741-26346193 | Common:2; Rare:139 | ||||
| chr2:26764183-26764373 | Common:2; Rare:71 | ||||
| chr2:26785779-26786092 | Rare:76 | ||||
| chr2:27032833-27033011 | Rare:74 | ||||
| chr2:27051546-27051689 | Rare:43 | ||||
| chr2:27071551-27071884 | Common:1; Rare:100 |