Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23319663-23320019 | Common:2; Rare:60 | ||||
chr1:23320447-23320495 | Rare:9 | ||||
chr1:23347327-23347467 | Rare:19 | ||||
chr1:23356367-23356417 | Rare:11 | ||||
chr1:23384393-23384653 | Rare:62 | ||||
chr1:23554933-23555282 | Rare:133 | ||||
chr1:23557634-23558224 | Common:5; Rare:182 | ||||
chr1:23558247-23558564 | Common:3; Rare:125 | ||||
chr1:23562213-23562666 | Common:1; Rare:111 | ||||
chr1:23635067-23635222 | Rare:36 | ||||
chr1:23693730-23694147 | Common:1; Rare:119; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:23695764-23696276 | Common:1; Rare:104; Clinvar (benign):1 | ||||
chr1:23744566-23744685 | Common:3; Rare:17 | ||||
chr1:23810698-23810968 | Rare:75; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:24007849-24007960 | Common:1; Rare:10 |