Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:121184907-121185088 | Rare:62 | ||||
chr1:121185157-121185368 | Rare:34 | ||||
chr1:121185530-121185848 | Rare:11 | ||||
chr1:145214903-145215043 | Rare:21 | ||||
chr1:145215251-145215281 | Rare:1 | ||||
chr1:145823848-145824251 | Rare:141 | ||||
chr1:145858994-145859217 | Rare:63 | ||||
chr1:145918686-145919034 | Common:2; Rare:76 | ||||
chr1:145927374-145927662 | Common:1; Rare:76; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958202 | Rare:47 | ||||
chr1:145964571-145964767 | Rare:48 | ||||
chr1:145995142-145995593 | Common:1; Rare:181 | ||||
chr1:145995809-145996006 | Common:2; Rare:61 | ||||
chr1:145996008-145996319 | Rare:141 | ||||
chr1:145996322-145996885 | Common:2; Rare:193 |