Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43367958-43368212 | Rare:67 | ||||
chr1:43389747-43389958 | Common:4; Rare:96 | ||||
chr1:43707332-43707571 | Common:2; Rare:72 | ||||
chr1:44775824-44776138 | Common:2; Rare:114 | ||||
chr1:45339996-45340212 | Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
chr1:45500025-45500341 | Common:2; Rare:75; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45583931-45584066 | Rare:51 | ||||
chr1:45688042-45688238 | Common:1; Rare:55 | ||||
chr1:46198358-46198506 | Common:1; Rare:58; Clinvar:1 | ||||
chr1:46303126-46303248 | Common:1; Rare:29 | ||||
chr1:46303308-46303740 | Common:2; Rare:116 | ||||
chr1:50970094-50970271 | Rare:33 | ||||
chr1:52055181-52055261 | Common:1; Rare:20 | ||||
chr1:52056169-52056336 | Rare:51 | ||||
chr1:52404438-52404624 | Common:1; Rare:54 |