Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94541622-94542011 | Common:1; Rare:111 | ||||
chr1:94820154-94820474 | Common:4; Rare:83 | ||||
chr1:94820555-94820683 | Common:2; Rare:29 | ||||
chr1:94903114-94903526 | Common:1; Rare:83 | ||||
chr1:94926842-94927192 | Common:3; Rare:107 | ||||
chr1:94927218-94927492 | Common:1; Rare:93 | ||||
chr1:95072863-95072995 | Common:1; Rare:52; Clinvar (benign):1 | ||||
chr1:95233933-95234256 | Common:5; Rare:100 | ||||
chr1:97920884-97921156 | Rare:108; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr1:98661564-98661875 | Common:2; Rare:108 | ||||
chr1:99646186-99646348 | Rare:40 | ||||
chr1:99850017-99850263 | Rare:76 | ||||
chr1:99850319-99850413 | Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
chr1:99969826-99970252 | Common:3; Rare:95 | ||||
chr1:100037973-100038148 | Common:1; Rare:71 |