| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:24952463-24952758 | Common:2; Rare:82 | ||||
| chr22:25405383-25405585 | Common:7; Rare:101 | ||||
| chr22:25564567-25564883 | Common:1; Rare:91 | ||||
| chr22:26429137-26429310 | Common:2; Rare:72 | ||||
| chr22:26483752-26483959 | Common:4; Rare:87; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512325-26512667 | Common:2; Rare:117 | ||||
| chr22:27919176-27919542 | Common:5; Rare:161 | ||||
| chr22:28725117-28725257 | Rare:47; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr22:28741767-28742090 | Common:2; Rare:108; Clinvar:5; Clinvar (benign):9 | ||||
| chr22:28742408-28742726 | Common:1; Rare:77 | ||||
| chr22:28800486-28800728 | Common:5; Rare:98 | ||||
| chr22:28883185-28883454 | Common:3; Rare:58 | ||||
| chr22:29205795-29206114 | Common:1; Rare:79 | ||||
| chr22:29267693-29268349 | Common:3; Rare:189 | ||||
| chr22:29306892-29307058 | Common:2; Rare:67 |