Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234608112-234608248 | Rare:43 | ||||
chr1:235128784-235129129 | Common:1; Rare:132 | ||||
chr1:235161168-235161430 | Common:1; Rare:163 | ||||
chr1:235327231-235327721 | Rare:212 | ||||
chr1:235328461-235328621 | Common:2; Rare:58 | ||||
chr1:235328771-235329069 | Common:1; Rare:94 | ||||
chr1:235329139-235329384 | Common:3; Rare:52 | ||||
chr1:235367251-235367478 | Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
chr1:235503764-235503868 | Common:1; Rare:17 | ||||
chr1:235504365-235504848 | Common:5; Rare:147 | ||||
chr1:235504969-235505157 | Rare:44 | ||||
chr1:235649810-235650360 | Common:6; Rare:143 | ||||
chr1:235866888-235867348 | Common:3; Rare:134 | ||||
chr1:236065047-236065329 | Common:2; Rare:111; Clinvar (pathogenic):1 | ||||
chr1:236281927-236282281 | Common:6; Rare:103 |