Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52906213-52906613 | Common:2; Rare:96 | ||||
chr1:52913566-52913966 | Common:6; Rare:149 | ||||
chr1:52926858-52927859 | Common:27; Rare:527; Clinvar:4 | ||||
chr1:53014720-53015070 | Rare:321; Clinvar:1; Clinvar (benign):1 | ||||
chr1:53015135-53015535 | Common:1; Rare:63 | ||||
chr1:53090820-53091220 | Common:10; Rare:167 | ||||
chr1:53196504-53197029 | Common:6; Rare:712; Clinvar:40; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr1:53196995-53197761 | Common:4; Rare:235; Clinvar:3; Clinvar (pathogenic):5 | ||||
chr1:53220159-53220440 | Rare:362 | ||||
chr1:53220443-53220855 | Common:11; Rare:509 | ||||
chr1:53238220-53238813 | Common:14; Rare:726 | ||||
chr1:53238815-53239215 | Rare:85 | ||||
chr1:53326985-53327496 | Common:19; Rare:274 | ||||
chr1:53327700-53328420 | Common:20; Rare:633 | ||||
chr1:53460300-53460700 | Common:4; Rare:321 |