| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46125263-46125617 | Common:4; Rare:191; Clinvar:20; Clinvar (benign):11; Clinvar (pathogenic):4 | ||||
| chr21:46129764-46130291 | Common:7; Rare:197 | ||||
| chr22:16601177-16601512 | Common:2; Rare:131 | ||||
| chr22:18068504-18068603 | Common:2; Rare:14 | ||||
| chr22:19171612-19171724 | Rare:35 | ||||
| chr22:19475586-19475849 | Rare:45 | ||||
| chr22:19758646-19758784 | Rare:41 | ||||
| chr22:22298046-22298196 | Common:2; Rare:62 | ||||
| chr22:23181703-23181790 | Common:1; Rare:44 | ||||
| chr22:26672663-26672786 | Common:2; Rare:32 | ||||
| chr22:29481010-29481125 | Common:1; Rare:48 | ||||
| chr22:30922240-30922355 | Common:1; Rare:47 | ||||
| chr22:30969035-30969292 | Common:2; Rare:73 | ||||
| chr22:31090158-31090636 | Common:3; Rare:92 | ||||
| chr22:31100704-31101048 | Common:2; Rare:95 |