Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:159923721-159923899 | Common:1; Rare:29 | ||||
chr1:159925452-159925617 | Common:1; Rare:43 | ||||
chr1:159945967-159946226 | Common:1; Rare:57 | ||||
chr1:160262436-160262636 | Common:1; Rare:64 | ||||
chr1:160343171-160343391 | Rare:88 | ||||
chr1:160400410-160400615 | Common:1; Rare:52 | ||||
chr1:161020863-161020938 | Rare:18 | ||||
chr1:161021101-161021507 | Common:2; Rare:108 | ||||
chr1:161045888-161046064 | Common:1; Rare:46 | ||||
chr1:161098288-161098383 | Common:1; Rare:15 | ||||
chr1:161117995-161118153 | Rare:86 | ||||
chr1:161132417-161132700 | Common:1; Rare:94 | ||||
chr1:161159392-161159520 | Common:1; Rare:34 | ||||
chr1:161166263-161166511 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161225768-161226082 | Common:10; Rare:45 |