Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153986111-153986592 | Common:1; Rare:119 | ||||
chr1:153990607-153990841 | Common:2; Rare:106 | ||||
chr1:154182987-154183298 | Rare:98 | ||||
chr1:154220509-154220986 | Common:1; Rare:159 | ||||
chr1:154272486-154272773 | Common:4; Rare:76; Clinvar:3; Clinvar (benign):3 | ||||
chr1:154501724-154501841 | Rare:43 | ||||
chr1:154868062-154868171 | Rare:21 | ||||
chr1:154936622-154936924 | Common:3; Rare:83 | ||||
chr1:154956078-154956235 | Common:1; Rare:45 | ||||
chr1:154961458-154961560 | Rare:27 | ||||
chr1:154961688-154962041 | Common:1; Rare:123 | ||||
chr1:154970709-154971048 | Common:1; Rare:77 | ||||
chr1:154974322-154974730 | Rare:104 | ||||
chr1:155051155-155051387 | Common:2; Rare:78 | ||||
chr1:155127760-155127937 | Common:1; Rare:36 |