Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243255320-243255556 | Rare:48 | ||||
chr1:243255776-243256122 | Rare:99; Clinvar:4 | ||||
chr1:243850130-243850470 | Common:2; Rare:106 | ||||
chr1:243850590-243850833 | Common:1; Rare:83 | ||||
chr1:243850884-243851284 | Common:5; Rare:189 | ||||
chr1:244048174-244048505 | Rare:114 | ||||
chr1:244050988-244051308 | Rare:41 | ||||
chr1:244451823-244452365 | Common:2; Rare:165 | ||||
chr1:244652937-244653173 | Common:3; Rare:96 | ||||
chr1:244653622-244654550 | Common:4; Rare:326 | ||||
chr1:244835172-244835365 | Rare:74 | ||||
chr1:244835551-244835722 | Common:2; Rare:74; Clinvar (benign):4 | ||||
chr1:244862897-244863370 | Common:13; Rare:394 | ||||
chr1:244864445-244864835 | Common:1; Rare:159 | ||||
chr1:244969680-244969817 | Rare:40 |