Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156130320-156130773 | Common:3; Rare:112; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:156503367-156503583 | Common:1; Rare:37 | ||||
chr1:156748344-156748484 | Common:2; Rare:25 | ||||
chr1:159012344-159012375 | Rare:5 | ||||
chr1:159012572-159012801 | Common:1; Rare:51 | ||||
chr1:159766048-159766265 | Common:2; Rare:32 | ||||
chr1:160294547-160294772 | Rare:44; Clinvar:1 | ||||
chr1:160297561-160297898 | Common:1; Rare:70 | ||||
chr1:161120426-161120554 | Rare:45 | ||||
chr1:161193244-161193579 | Common:1; Rare:97 | ||||
chr1:161198159-161198459 | Common:3; Rare:105 | ||||
chr1:161200051-161200231 | Rare:26 | ||||
chr1:161201142-161201303 | Common:2; Rare:21 | ||||
chr1:161207229-161207504 | Common:1; Rare:60 | ||||
chr1:161216981-161217264 | Rare:47 |