Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145859750-145859928 | Common:2; Rare:62 | ||||
chr1:145885823-145886014 | Rare:37 | ||||
chr1:145918671-145919005 | Common:2; Rare:76; Clinvar:1 | ||||
chr1:145927422-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958279 | Rare:61 | ||||
chr1:145964573-145964742 | Rare:43 | ||||
chr1:146228968-146229180 | Common:2; Rare:46 | ||||
chr1:147172420-147172823 | Common:1; Rare:103 | ||||
chr1:148951284-148951522 | Common:3; Rare:40 | ||||
chr1:148951991-148952169 | Common:3; Rare:51 | ||||
chr1:148952237-148952642 | Common:5; Rare:107 | ||||
chr1:149842746-149842968 | Rare:3 | ||||
chr1:149850848-149851063 | Rare:1 | ||||
chr1:149886668-149887031 | Common:2; Rare:127 | ||||
chr1:149887941-149888215 | Rare:65 |