| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46635136-46635166 | Rare:3 | ||||
| chr22:17159136-17159385 | Common:7; Rare:115 | ||||
| chr22:17198365-17198636 | Common:3; Rare:42 | ||||
| chr22:17628675-17628897 | Common:1; Rare:85 | ||||
| chr22:17638668-17638830 | Rare:58 | ||||
| chr22:17774398-17774665 | Rare:78 | ||||
| chr22:18024463-18024641 | Common:1; Rare:53 | ||||
| chr22:18024839-18025031 | Common:3; Rare:30 | ||||
| chr22:18077672-18078058 | Common:5; Rare:100; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19122389-19122669 | Common:3; Rare:65 | ||||
| chr22:19178449-19178508 | Common:1; Rare:14 | ||||
| chr22:19431537-19431836 | Common:1; Rare:84 | ||||
| chr22:19432284-19432567 | Common:3; Rare:115 | ||||
| chr22:19447663-19447967 | Common:2; Rare:127 | ||||
| chr22:19479107-19479471 | Common:4; Rare:135 |