Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:226939991-226940345 | Rare:121; Clinvar:3 | ||||
chr1:227735269-227735477 | Common:2; Rare:120 | ||||
chr1:228103317-228103374 | Rare:16 | ||||
chr1:228109240-228109468 | Rare:80 | ||||
chr1:228457866-228458113 | Common:1; Rare:78 | ||||
chr1:229271027-229271293 | Rare:90 | ||||
chr1:229508278-229508429 | Common:1; Rare:63 | ||||
chr1:229625962-229626205 | Rare:67 | ||||
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 | ||||
chr1:236065037-236065314 | Common:2; Rare:110; Clinvar (pathogenic):1 | ||||
chr1:236281936-236282249 | Common:6; Rare:91 | ||||
chr1:241848129-241848233 | Common:1; Rare:19 | ||||
chr1:243255201-243255422 | Common:1; Rare:49 |