Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145858996-145859144 | Rare:43 | ||||
chr1:145918665-145918987 | Common:2; Rare:73; Clinvar:1 | ||||
chr1:145927354-145927607 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
chr1:145964571-145964748 | Rare:46 | ||||
chr1:145996093-145996397 | Rare:118 | ||||
chr1:147172429-147172786 | Common:1; Rare:92 | ||||
chr1:147670442-147670646 | Common:2; Rare:38 | ||||
chr1:149390431-149390663 | Rare:33 | ||||
chr1:149812363-149812611 | Common:1; Rare:67 | ||||
chr1:149886639-149886971 | Common:2; Rare:124 | ||||
chr1:149887961-149888215 | Rare:50 | ||||
chr1:149927757-149927922 | Common:1; Rare:67; Clinvar (benign):5 | ||||
chr1:150067651-150067858 | Rare:62 | ||||
chr1:150149413-150149682 | Rare:51 | ||||
chr1:150268279-150268434 | Rare:27 |