Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1780011-1780310 | Common:1; Rare:59 | ||||
chr1:1890823-1891194 | Rare:133 | ||||
chr1:1891389-1891549 | Common:2; Rare:18 | ||||
chr1:2019142-2019365 | Common:3; Rare:41 | ||||
chr1:2050174-2050513 | Common:2; Rare:132 | ||||
chr1:2194725-2195098 | Rare:96 | ||||
chr1:2391543-2391934 | Common:2; Rare:140 | ||||
chr1:2412492-2412791 | Common:2; Rare:126; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:2413778-2414005 | Rare:61 | ||||
chr1:2526588-2526753 | Common:3; Rare:61 | ||||
chr1:2586419-2586889 | Common:3; Rare:112 | ||||
chr1:3454477-3454741 | Common:1; Rare:70 | ||||
chr1:3624720-3625086 | Common:1; Rare:114 | ||||
chr1:3772441-3772787 | Common:3; Rare:78 | ||||
chr1:3796442-3796564 | Common:3; Rare:54 |