Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63523981-63523993 | Rare:3 | ||||
chr1:63593588-63593816 | Common:1; Rare:115; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr1:63594180-63594219 | Common:1; Rare:7 | ||||
chr1:63773880-63774086 | Rare:37 | ||||
chr1:63775127-63775311 | Common:2; Rare:49 | ||||
chr1:64469929-64470326 | Common:3; Rare:95 | ||||
chr1:64470367-64470423 | Rare:16 | ||||
chr1:64470540-64470612 | Rare:19 | ||||
chr1:64744526-64744738 | Common:1; Rare:51 | ||||
chr1:64744764-64745197 | Common:2; Rare:121 | ||||
chr1:64745285-64745348 | Common:1; Rare:19 | ||||
chr1:64966425-64966781 | Common:3; Rare:131 | ||||
chr1:64966921-64967243 | Common:1; Rare:55 | ||||
chr1:65147388-65147623 | Rare:70 | ||||
chr1:65148722-65148994 | Common:2; Rare:73 |