Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43649842-43650191 | Rare:85 | ||||
chr1:43946585-43946983 | Rare:105 | ||||
chr1:43974796-43975046 | Common:3; Rare:69 | ||||
chr1:44017144-44017303 | Rare:46 | ||||
chr1:44213357-44213504 | Common:1; Rare:29 | ||||
chr1:44405204-44405308 | Rare:28 | ||||
chr1:44674406-44674749 | Common:3; Rare:92 | ||||
chr1:44739648-44739887 | Common:2; Rare:91 | ||||
chr1:44775445-44775599 | Rare:59 | ||||
chr1:44775838-44776138 | Common:2; Rare:108 | ||||
chr1:44986532-44986850 | Common:2; Rare:65; Clinvar (benign):1 | ||||
chr1:45012085-45012284 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45339974-45340041 | Rare:19 | ||||
chr1:45340109-45340223 | Rare:53; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:45340386-45340502 | Common:1; Rare:31; Clinvar:1 |