Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26692516-26692657 | Common:4; Rare:71 | ||||
chr1:26692939-26693361 | Common:3; Rare:287 | ||||
chr1:26694764-26695136 | Rare:97 | ||||
chr1:26697001-26697115 | Rare:49 | ||||
chr1:26697127-26697541 | Common:1; Rare:275; Clinvar:7; Clinvar (benign):4 | ||||
chr1:26697855-26698630 | Rare:327 | ||||
chr1:26722460-26723664 | Common:4; Rare:255 | ||||
chr1:26742159-26742620 | Common:2; Rare:118 | ||||
chr1:26744220-26744457 | Common:1; Rare:60 | ||||
chr1:26790520-26790958 | Rare:158; Clinvar:6; Clinvar (pathogenic):2 | ||||
chr1:26827630-26828269 | Common:6; Rare:218 | ||||
chr1:26828279-26828700 | Common:6; Rare:129 | ||||
chr1:26828789-26828975 | Common:1; Rare:35 | ||||
chr1:26833531-26833785 | Rare:91 | ||||
chr1:26838960-26839310 | Common:1; Rare:67 |