Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228457824-228458114 | Common:1; Rare:116 | ||||
chr1:229271027-229271307 | Rare:93 | ||||
chr1:229508267-229508440 | Common:1; Rare:70 | ||||
chr1:229625938-229626274 | Rare:109 | ||||
chr1:231241107-231241362 | Common:2; Rare:126; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231528515-231528738 | Common:2; Rare:79 | ||||
chr1:234373387-234373775 | Common:1; Rare:177; Clinvar (benign):7 | ||||
chr1:234608052-234608351 | Common:1; Rare:97 | ||||
chr1:235128767-235129105 | Common:1; Rare:132 | ||||
chr1:235328116-235328454 | Common:2; Rare:96 | ||||
chr1:235328480-235328584 | Common:1; Rare:31 | ||||
chr1:235866850-235867178 | Common:3; Rare:103 | ||||
chr1:236064931-236064963 | Rare:9 | ||||
chr1:236064966-236065326 | Common:3; Rare:130; Clinvar (pathogenic):1 | ||||
chr1:236523794-236524034 | Common:4; Rare:64 |