Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:217957249-217957388 | Common:4; Rare:23 | ||||
chr2:218272449-218272617 | Rare:53 | ||||
chr2:218402615-218402714 | Rare:37 | ||||
chr2:219420816-219421208 | Common:1; Rare:81; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
chr2:219423763-219423893 | Rare:38; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr2:219433995-219434292 | Rare:57 | ||||
chr2:219462044-219462349 | Rare:75 | ||||
chr2:226796032-226796227 | Common:1; Rare:69 | ||||
chr2:226796864-226797120 | Rare:79; Clinvar (pathogenic):1 | ||||
chr2:231666427-231666652 | Rare:53 | ||||
chr2:237314259-237314471 | Common:1; Rare:52 | ||||
chr2:237898735-237898912 | Common:3; Rare:42 | ||||
chr2:238286707-238286917 | Common:1; Rare:36 | ||||
chr2:239280228-239280476 | Common:2; Rare:56 | ||||
chr2:239348800-239348941 | Rare:30 |