Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235328821-235329018 | Common:1; Rare:61 | ||||
chr1:235866858-235867126 | Common:3; Rare:79 | ||||
chr1:236065037-236065356 | Common:3; Rare:120; Clinvar (pathogenic):1 | ||||
chr1:240612114-240612199 | Rare:20 | ||||
chr1:241848100-241848245 | Common:2; Rare:32 | ||||
chr1:243255040-243255428 | Common:1; Rare:93 | ||||
chr1:243255741-243256117 | Rare:103; Clinvar:4 | ||||
chr1:244050959-244051392 | Rare:67 | ||||
chr1:244835142-244835333 | Rare:77 | ||||
chr1:244835575-244835741 | Common:2; Rare:73; Clinvar (benign):4 | ||||
chr1:244864264-244864686 | Rare:157 | ||||
chr1:244970251-244970413 | Common:3; Rare:76 | ||||
chr1:246566160-246566519 | Common:2; Rare:125 | ||||
chr1:246724245-246724414 | Common:1; Rare:66 | ||||
chr1:247078739-247078896 | Rare:49 |