Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24319367-24319495 | Rare:27 | ||||
chr1:24413691-24413855 | Common:1; Rare:36 | ||||
chr1:24415515-24415868 | Common:3; Rare:83 | ||||
chr1:24502392-24502569 | Common:1; Rare:42 | ||||
chr1:24555893-24556149 | Common:3; Rare:67 | ||||
chr1:24642880-24643344 | Common:2; Rare:154 | ||||
chr1:24745089-24745622 | Common:3; Rare:186 | ||||
chr1:25232444-25232662 | Rare:88 | ||||
chr1:25247318-25247638 | Common:2; Rare:124 | ||||
chr1:25337833-25337954 | Rare:15 | ||||
chr1:25338188-25338532 | Common:2; Rare:117 | ||||
chr1:25543463-25543676 | Common:1; Rare:78; Clinvar:5 | ||||
chr1:25813767-25813907 | Rare:38; Clinvar (pathogenic):3 | ||||
chr1:25819853-25820054 | Common:5; Rare:65 | ||||
chr1:25820806-25820953 | Common:2; Rare:34 |