Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44775838-44776140 | Common:2; Rare:109 | ||||
chr1:45340118-45340182 | Rare:24 | ||||
chr1:45499987-45500356 | Common:2; Rare:87; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521827-45522000 | Common:1; Rare:72 | ||||
chr1:45550741-45551094 | Common:3; Rare:83 | ||||
chr1:45583927-45584164 | Rare:95 | ||||
chr1:45687059-45687211 | Common:1; Rare:49 | ||||
chr1:45688055-45688243 | Common:1; Rare:54 | ||||
chr1:45913351-45913723 | Rare:69 | ||||
chr1:46132614-46132812 | Rare:70 | ||||
chr1:46133013-46133209 | Common:1; Rare:44 | ||||
chr1:46198358-46198518 | Common:1; Rare:63; Clinvar:1 | ||||
chr1:46303138-46303294 | Common:1; Rare:51 | ||||
chr1:46303296-46303820 | Common:2; Rare:147 | ||||
chr1:46604233-46604392 | Rare:44 |