Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235329111-235329806 | Common:7; Rare:235 | ||||
chr1:235367124-235367874 | Common:7; Rare:377; Clinvar:10; Clinvar (benign):9 | ||||
chr1:235441337-235441737 | Rare:109 | ||||
chr1:235504198-235504351 | Rare:52; Clinvar:2; Clinvar (benign):3 | ||||
chr1:235504367-235504870 | Common:30; Rare:765 | ||||
chr1:235504820-235505431 | Common:4; Rare:234 | ||||
chr1:235588894-235589300 | Common:2; Rare:151 | ||||
chr1:235589250-235589650 | Common:2; Rare:159 | ||||
chr1:235866793-235867247 | Common:15; Rare:531 | ||||
chr1:235867353-235867753 | Common:2; Rare:75 | ||||
chr1:236142180-236142570 | Common:7; Rare:83 | ||||
chr1:236281353-236281753 | Common:3; Rare:121 | ||||
chr1:236281826-236282325 | Common:44; Rare:748 | ||||
chr1:236394050-236394495 | Common:4; Rare:175; Clinvar (benign):3 | ||||
chr1:236394919-236396341 | Common:14; Rare:844 |