| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74178767-74179100 | Common:5; Rare:102 | ||||
| chr2:74198275-74198785 | Common:10; Rare:181 | ||||
| chr2:74198909-74199383 | Common:3; Rare:110 | ||||
| chr2:74391588-74391776 | Common:3; Rare:58 | ||||
| chr2:74391782-74392177 | Common:2; Rare:177 | ||||
| chr2:74421409-74421786 | Rare:107 | ||||
| chr2:74422082-74422220 | Rare:58 | ||||
| chr2:74440399-74441236 | Rare:161 | ||||
| chr2:74441859-74442437 | Common:5; Rare:107 | ||||
| chr2:74442454-74442569 | Rare:19 | ||||
| chr2:74454763-74455144 | Rare:89 | ||||
| chr2:74457895-74457980 | Rare:23 | ||||
| chr2:74457992-74458520 | Common:1; Rare:161 | ||||
| chr2:74465198-74465553 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:74472092-74472298 | Rare:80 |