Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119648138-119648372 | Common:3; Rare:79 | ||||
chr1:120176338-120176593 | Rare:56 | ||||
chr1:120914087-120914230 | Rare:17 | ||||
chr1:144461550-144461694 | Common:5; Rare:67 | ||||
chr1:145214908-145215036 | Rare:19 | ||||
chr1:145607851-145608075 | Common:2; Rare:67 | ||||
chr1:145823882-145824268 | Rare:139 | ||||
chr1:145845838-145846026 | Rare:68 | ||||
chr1:145858996-145859179 | Rare:53 | ||||
chr1:145859741-145859996 | Common:3; Rare:77 | ||||
chr1:145918671-145919043 | Common:2; Rare:87; Clinvar:1 | ||||
chr1:145927358-145927644 | Common:1; Rare:74; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958224 | Rare:52 | ||||
chr1:145964571-145964768 | Rare:48 | ||||
chr1:145996472-145996848 | Common:2; Rare:150 |