Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44799620-44800020 | Common:3; Rare:72 | ||||
chr1:44800153-44800405 | Common:2; Rare:61 | ||||
chr1:44986534-44986852 | Common:2; Rare:65; Clinvar (benign):1 | ||||
chr1:45011325-45011426 | Rare:23 | ||||
chr1:45012130-45012284 | Common:1; Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45012681-45012814 | Common:1; Rare:25 | ||||
chr1:45206573-45206788 | Common:1; Rare:73 | ||||
chr1:45339553-45339736 | Rare:33 | ||||
chr1:45339777-45340259 | Common:2; Rare:169; Clinvar:13; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr1:45340387-45340608 | Common:1; Rare:51; Clinvar:1 | ||||
chr1:45340872-45341161 | Common:1; Rare:73 | ||||
chr1:45491062-45491376 | Common:3; Rare:86 | ||||
chr1:45499921-45500492 | Common:2; Rare:148; Clinvar:6; Clinvar (pathogenic):6 | ||||
chr1:45521824-45522140 | Common:1; Rare:124 | ||||
chr1:45522757-45522869 | Rare:19 |