| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:36291689-36292273 | Common:3; Rare:161; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:36293128-36293511 | Rare:91; Clinvar:5 | ||||
| chr22:36293759-36294322 | Common:5; Rare:172; Clinvar:6; Clinvar (benign):8 | ||||
| chr22:36305810-36306054 | Common:2; Rare:68; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:36317613-36317910 | Common:1; Rare:85 | ||||
| chr22:36320385-36320534 | Common:2; Rare:32 | ||||
| chr22:36323392-36323521 | Rare:21 | ||||
| chr22:36324459-36324708 | Common:1; Rare:43 | ||||
| chr22:36325327-36325406 | Rare:19 | ||||
| chr22:36330537-36330860 | Common:2; Rare:62 | ||||
| chr22:36331070-36331254 | Common:2; Rare:34 | ||||
| chr22:36331569-36331760 | Common:3; Rare:36 | ||||
| chr22:36332368-36332456 | Common:1; Rare:16 | ||||
| chr22:36332632-36332712 | Common:1; Rare:16 | ||||
| chr22:36340694-36340857 | Rare:41 |