Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145858992-145859175 | Rare:51 | ||||
chr1:145918662-145919022 | Common:2; Rare:90; Clinvar:1 | ||||
chr1:145927394-145927623 | Common:1; Rare:61; Clinvar (pathogenic):1 | ||||
chr1:145957996-145958204 | Rare:48 | ||||
chr1:145964571-145964726 | Rare:38 | ||||
chr1:145995325-145995485 | Rare:65 | ||||
chr1:147172438-147172744 | Common:1; Rare:80 | ||||
chr1:147225326-147225545 | Common:3; Rare:42 | ||||
chr1:148951845-148952153 | Common:5; Rare:73 | ||||
chr1:148952271-148952603 | Common:5; Rare:100 | ||||
chr1:149886612-149887113 | Common:3; Rare:193 | ||||
chr1:149887116-149887189 | Rare:29 | ||||
chr1:149887947-149888215 | Rare:62 | ||||
chr1:149899340-149899597 | Common:3; Rare:49 | ||||
chr1:149927767-149927900 | Common:1; Rare:51; Clinvar (benign):4 |