| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61144916-61145176 | Common:3; Rare:84 | ||||
| chr2:61177158-61177472 | Common:6; Rare:126 | ||||
| chr2:61470652-61471029 | Common:1; Rare:122 | ||||
| chr2:61471226-61471390 | Common:3; Rare:59 | ||||
| chr2:61536740-61536857 | Rare:39 | ||||
| chr2:61537060-61537115 | Rare:12 | ||||
| chr2:61537734-61537866 | Rare:34 | ||||
| chr2:61538166-61538439 | Common:1; Rare:66 | ||||
| chr2:61538690-61538779 | Rare:25 | ||||
| chr2:61853955-61854105 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61854493-61854686 | Rare:36 | ||||
| chr2:61888309-61888345 | Rare:8 | ||||
| chr2:61888379-61888713 | Common:1; Rare:150 | ||||
| chr2:61905577-61905714 | Rare:61 | ||||
| chr2:62506130-62506385 | Common:1; Rare:97 |