Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119648126-119648356 | Common:3; Rare:80 | ||||
chr1:121184807-121185062 | Common:1; Rare:91 | ||||
chr1:145214759-145215004 | Rare:28 | ||||
chr1:145607825-145608105 | Common:2; Rare:85 | ||||
chr1:145823869-145824088 | Rare:80 | ||||
chr1:145824091-145824296 | Rare:63 | ||||
chr1:145918686-145919013 | Common:2; Rare:70 | ||||
chr1:145927358-145927644 | Common:1; Rare:74; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958202 | Rare:46 | ||||
chr1:145964571-145964759 | Rare:47 | ||||
chr1:145996534-145996845 | Common:1; Rare:126 | ||||
chr1:146021682-146021841 | Rare:34; Clinvar:1 | ||||
chr1:146228961-146229170 | Common:2; Rare:48 | ||||
chr1:146938315-146938519 | Common:2; Rare:61 | ||||
chr1:147172427-147172823 | Common:1; Rare:102 |