| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43776276-43776611 | Common:4; Rare:119; Clinvar:2; Clinvar (benign):8 | ||||
| chr21:44873622-44874032 | Common:8; Rare:166 | ||||
| chr21:45981530-45981813 | Common:23; Rare:63; Clinvar (benign):2 | ||||
| chr21:46286280-46286399 | Common:2; Rare:37 | ||||
| chr22:17084824-17085005 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:17628615-17628822 | Common:2; Rare:68 | ||||
| chr22:19432345-19432599 | Common:2; Rare:110 | ||||
| chr22:19941746-19942124 | Common:2; Rare:100; Clinvar:4 | ||||
| chr22:20117212-20117587 | Common:3; Rare:122 | ||||
| chr22:20319995-20320158 | Common:2; Rare:53 | ||||
| chr22:20495787-20495994 | Common:2; Rare:77 | ||||
| chr22:20858744-20859088 | Common:4; Rare:173; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:24555035-24555484 | Common:4; Rare:164 | ||||
| chr22:24555889-24556007 | Rare:31 | ||||
| chr22:26512444-26512536 | Common:1; Rare:43 |