Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25247398-25247638 | Common:2; Rare:95 | ||||
chr1:25272280-25272550 | Rare:31 | ||||
chr1:25337838-25337944 | Rare:12 | ||||
chr1:25338190-25338453 | Common:1; Rare:93 | ||||
chr1:25420787-25420935 | Common:2; Rare:23 | ||||
chr1:25819878-25820029 | Common:3; Rare:47 | ||||
chr1:25859353-25859612 | Common:3; Rare:108 | ||||
chr1:26234142-26234244 | Common:1; Rare:41 | ||||
chr1:26279934-26280173 | Rare:133 | ||||
chr1:26432099-26432422 | Common:5; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472213-26472539 | Common:4; Rare:109 | ||||
chr1:26545712-26545873 | Common:1; Rare:34 | ||||
chr1:26786952-26787058 | Rare:25 | ||||
chr1:26787877-26788243 | Common:3; Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890235-26890377 | Common:1; Rare:61 |