| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:234978521-234978747 | Common:3; Rare:48 | ||||
| chr2:237085819-237085951 | Common:1; Rare:55 | ||||
| chr2:237487141-237487346 | Common:3; Rare:55 | ||||
| chr2:237966728-237967039 | Common:3; Rare:91 | ||||
| chr2:238060738-238061022 | Common:4; Rare:87 | ||||
| chr2:238203569-238203821 | Common:5; Rare:104 | ||||
| chr2:238426893-238427009 | Common:1; Rare:39 | ||||
| chr2:239401641-239401739 | Rare:45 | ||||
| chr2:240025282-240025581 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136274-240136357 | Rare:36 | ||||
| chr2:240456677-240456948 | Rare:76 | ||||
| chr2:240465244-240465632 | Common:4; Rare:135 | ||||
| chr2:240465909-240466057 | Common:2; Rare:46 | ||||
| chr2:240560764-240560906 | Common:2; Rare:65 | ||||
| chr2:241051113-241051282 | Rare:32 |