Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:147670433-147670737 | Common:2; Rare:73 | ||||
chr1:148458709-148459017 | Common:2; Rare:88 | ||||
chr1:148459196-148459475 | Rare:77 | ||||
chr1:149103448-149103731 | Common:7; Rare:108 | ||||
chr1:149390406-149390693 | Rare:47 | ||||
chr1:149811158-149811497 | Common:4; Rare:78 | ||||
chr1:149812259-149812609 | Common:3; Rare:139 | ||||
chr1:149886641-149886975 | Common:2; Rare:126 | ||||
chr1:149887915-149888232 | Rare:92 | ||||
chr1:149899446-149899661 | Common:3; Rare:46 | ||||
chr1:149927741-149927981 | Common:1; Rare:95; Clinvar (benign):5 | ||||
chr1:149928223-149928413 | Common:1; Rare:38 | ||||
chr1:149936821-149936954 | Common:1; Rare:27 | ||||
chr1:150010630-150010945 | Common:2; Rare:85 | ||||
chr1:150066917-150067322 | Common:4; Rare:73 |