Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23793530-23793669 | Rare:35 | ||||
chr1:23799485-23800017 | Common:1; Rare:105 | ||||
chr1:23800143-23800343 | Rare:44 | ||||
chr1:23800378-23801023 | Common:2; Rare:194; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23801296-23801363 | Rare:16 | ||||
chr1:23825139-23825187 | Rare:7 | ||||
chr1:23825328-23825627 | Common:3; Rare:91; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr1:23868251-23868537 | Common:6; Rare:78; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23959027-23959187 | Common:3; Rare:32 | ||||
chr1:23959196-23959447 | Common:1; Rare:56 | ||||
chr1:23959495-23959866 | Common:5; Rare:92 | ||||
chr1:23959906-23960226 | Common:1; Rare:80 | ||||
chr1:23960425-23960606 | Common:1; Rare:27 | ||||
chr1:23979767-23979907 | Common:2; Rare:34 | ||||
chr1:23980006-23980129 | Common:2; Rare:19 |