Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43946522-43946974 | Rare:125 | ||||
chr1:43974749-43974979 | Common:3; Rare:66 | ||||
chr1:44213320-44213501 | Common:1; Rare:36 | ||||
chr1:44405234-44405266 | Rare:8 | ||||
chr1:44405759-44406079 | Common:1; Rare:78 | ||||
chr1:44723697-44723832 | Rare:27 | ||||
chr1:44724630-44724839 | Rare:81 | ||||
chr1:44775776-44776138 | Common:2; Rare:132 | ||||
chr1:44777586-44777973 | Common:2; Rare:105 | ||||
chr1:44986540-44986791 | Common:2; Rare:48; Clinvar (benign):1 | ||||
chr1:45011887-45012266 | Common:5; Rare:102; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45339582-45339757 | Rare:37 | ||||
chr1:45339987-45340174 | Rare:57 | ||||
chr1:45340388-45340480 | Common:1; Rare:23; Clinvar:1 | ||||
chr1:45500017-45500350 | Common:2; Rare:80; Clinvar:4; Clinvar (pathogenic):3 |