Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:119648105-119648359 | Common:3; Rare:91 | ||||
chr1:120176352-120176598 | Rare:53 | ||||
chr1:145823922-145824268 | Rare:123 | ||||
chr1:145858996-145859175 | Rare:51 | ||||
chr1:145918680-145919022 | Common:2; Rare:79 | ||||
chr1:145927402-145927644 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
chr1:145957996-145958223 | Rare:53 | ||||
chr1:145964615-145964742 | Rare:30 | ||||
chr1:147172403-147172823 | Common:1; Rare:111 | ||||
chr1:148952020-148952623 | Common:8; Rare:159 | ||||
chr1:149812181-149812523 | Common:2; Rare:160 | ||||
chr1:149842745-149842939 | Rare:3 | ||||
chr1:149850826-149851062 | Rare:1 | ||||
chr1:149886632-149887145 | Common:3; Rare:200 | ||||
chr1:149887787-149888215 | Rare:141 |