Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:232950436-232950682 | Common:3; Rare:89 | ||||
chr1:234373321-234373775 | Common:1; Rare:206; Clinvar (benign):7 | ||||
chr1:234608194-234608247 | Rare:18 | ||||
chr1:235128703-235128951 | Rare:103 | ||||
chr1:235160998-235161335 | Common:2; Rare:175 | ||||
chr1:235327900-235328111 | Rare:57 | ||||
chr1:235328143-235328657 | Common:5; Rare:158 | ||||
chr1:235866852-235867107 | Common:3; Rare:77 | ||||
chr1:236064892-236065376 | Common:4; Rare:168; Clinvar (pathogenic):1 | ||||
chr1:236281936-236282258 | Common:6; Rare:95 | ||||
chr1:236523898-236524060 | Common:2; Rare:44 | ||||
chr1:236795117-236795501 | Common:5; Rare:159; Clinvar:4 | ||||
chr1:236795667-236795715 | Rare:28; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:240612066-240612158 | Rare:22 | ||||
chr1:241848094-241848232 | Common:1; Rare:29 |