Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243255047-243255358 | Common:1; Rare:69 | ||||
chr1:243255755-243256128 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451824-244452038 | Rare:65 | ||||
chr1:244864391-244864718 | Common:1; Rare:130 | ||||
chr1:244970255-244970421 | Common:3; Rare:74 | ||||
chr1:246565885-246565968 | Common:1; Rare:27 | ||||
chr1:246566149-246566584 | Common:2; Rare:149 | ||||
chr1:247078765-247078913 | Rare:37 | ||||
chr1:247104326-247104556 | Common:2; Rare:69 | ||||
chr10:988289-988502 | Common:1; Rare:85 | ||||
chr10:1048865-1049099 | Common:2; Rare:119 | ||||
chr10:1049115-1049179 | Common:1; Rare:17 | ||||
chr10:1056749-1056857 | Common:3; Rare:43 | ||||
chr10:3785165-3785551 | Common:4; Rare:140 | ||||
chr10:5813236-5813464 | Common:3; Rare:80 |