Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44674442-44674777 | Common:2; Rare:82 | ||||
chr1:45500078-45500351 | Common:1; Rare:69; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521882-45522013 | Common:1; Rare:49 | ||||
chr1:45583931-45584046 | Rare:42 | ||||
chr1:45688055-45688216 | Common:1; Rare:41 | ||||
chr1:46198368-46198517 | Common:1; Rare:58; Clinvar:1 | ||||
chr1:46303308-46303733 | Common:2; Rare:112 | ||||
chr1:50970073-50970271 | Rare:35 | ||||
chr1:52056144-52056335 | Rare:60 | ||||
chr1:53238470-53238592 | Rare:55 | ||||
chr1:53946276-53946509 | Common:2; Rare:83 | ||||
chr1:54053190-54053687 | Common:6; Rare:161 | ||||
chr1:54199971-54200199 | Rare:45 | ||||
chr1:63523201-63523247 | Common:2; Rare:13 | ||||
chr1:63593515-63593705 | Rare:95; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 |