| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25673391-25673816 | Common:1; Rare:150 | ||||
| chr2:25878194-25878242 | Rare:17 | ||||
| chr2:25878355-25878827 | Common:5; Rare:132 | ||||
| chr2:25982140-25982269 | Common:1; Rare:25 | ||||
| chr2:25982406-25982636 | Common:1; Rare:58 | ||||
| chr2:25982657-25982826 | Rare:38 | ||||
| chr2:26033401-26033763 | Common:1; Rare:95 | ||||
| chr2:26033868-26034203 | Common:1; Rare:110 | ||||
| chr2:26172930-26173146 | Rare:48 | ||||
| chr2:26242794-26242879 | Common:4; Rare:17 | ||||
| chr2:26243150-26243253 | Rare:20 | ||||
| chr2:26244590-26245006 | Common:2; Rare:150; Clinvar:6; Clinvar (benign):8 | ||||
| chr2:26345096-26345390 | Common:1; Rare:53 | ||||
| chr2:26345547-26345673 | Common:2; Rare:28 | ||||
| chr2:26345718-26346226 | Common:2; Rare:155 |