Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:24208722-24208973 | Common:2; Rare:69 | ||||
chr10:24209015-24209184 | Rare:50 | ||||
chr10:25016275-25016668 | Common:9; Rare:122 | ||||
chr10:27100419-27100630 | Common:4; Rare:61; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154249-27154480 | Rare:63 | ||||
chr10:27155170-27155439 | Common:7; Rare:115; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240466-27240910 | Common:2; Rare:126 | ||||
chr10:27242058-27242237 | Common:1; Rare:76 | ||||
chr10:27504026-27504193 | Rare:48; Clinvar:1 | ||||
chr10:27504202-27504367 | Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
chr10:27998825-27998899 | Rare:17 | ||||
chr10:28532480-28532868 | Common:5; Rare:154 | ||||
chr10:28533012-28533197 | Rare:76 | ||||
chr10:28533610-28533792 | Rare:92 | ||||
chr10:28677210-28677544 | Common:6; Rare:146 |