| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43226310-43226540 | Common:2; Rare:186 | ||||
| chr2:43226568-43226890 | Common:6; Rare:250 | ||||
| chr2:43595924-43596216 | Common:2; Rare:183 | ||||
| chr2:43995943-43996342 | Common:10; Rare:339; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:44167840-44168280 | Common:8; Rare:301 | ||||
| chr2:44168554-44168905 | Common:1; Rare:104 | ||||
| chr2:44361479-44362129 | Common:8; Rare:393 | ||||
| chr2:45009331-45009723 | Common:1; Rare:179 | ||||
| chr2:45611149-45611700 | Common:4; Rare:290 | ||||
| chr2:45650740-45651351 | Common:7; Rare:255 | ||||
| chr2:45651460-45651740 | Common:3; Rare:100 | ||||
| chr2:46073060-46073651 | Common:2; Rare:161 | ||||
| chr2:46073667-46073950 | Common:3; Rare:84 | ||||
| chr2:46297105-46297431 | Common:11; Rare:238 | ||||
| chr2:46297650-46297842 | Rare:71; Clinvar:5; Clinvar (benign):1 |