Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23800508-23801023 | Common:1; Rare:161 | ||||
chr1:23825299-23825579 | Common:3; Rare:99; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr1:23825895-23826136 | Common:1; Rare:44 | ||||
chr1:23868215-23868604 | Common:6; Rare:97; Clinvar:2; Clinvar (benign):5 | ||||
chr1:23913322-23913494 | Rare:32 | ||||
chr1:23959029-23959404 | Common:4; Rare:79 | ||||
chr1:23959522-23959854 | Common:5; Rare:83 | ||||
chr1:23959989-23960095 | Rare:38 | ||||
chr1:23960161-23960466 | Common:3; Rare:70 | ||||
chr1:23979900-23980066 | Common:4; Rare:49 | ||||
chr1:23980231-23980655 | Common:1; Rare:115 | ||||
chr1:23980822-23981035 | Common:1; Rare:40 | ||||
chr1:23981066-23981330 | Common:2; Rare:53 | ||||
chr1:24187217-24187449 | Common:9; Rare:68 | ||||
chr1:24413610-24413887 | Common:3; Rare:66 |