Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26036431-26036487 | Rare:9 | ||||
chr1:26698232-26698526 | Rare:81 | ||||
chr1:28247184-28247462 | Common:2; Rare:60 | ||||
chr1:28581869-28581961 | Common:1; Rare:29 | ||||
chr1:28648302-28648629 | Common:5; Rare:114 | ||||
chr1:31372219-31372310 | Common:1; Rare:19 | ||||
chr1:32612150-32612435 | Common:1; Rare:62 | ||||
chr1:33346974-33347244 | Common:1; Rare:48 | ||||
chr1:36175542-36175706 | Common:1; Rare:22 | ||||
chr1:39410960-39411113 | Rare:31 | ||||
chr1:39441005-39441324 | Rare:80 | ||||
chr1:39632947-39633256 | Common:1; Rare:73 | ||||
chr1:41423781-41424045 | Common:3; Rare:60 | ||||
chr1:41432916-41433197 | Common:2; Rare:58 | ||||
chr1:42929761-42929929 | Common:1; Rare:43; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):5 |