Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94926731-94926893 | Common:1; Rare:50 | ||||
chr1:94926907-94927278 | Common:4; Rare:121 | ||||
chr1:95072568-95072742 | Rare:48 | ||||
chr1:95072839-95073080 | Common:4; Rare:88; Clinvar (benign):2 | ||||
chr1:95116749-95116918 | Rare:32 | ||||
chr1:95117289-95117535 | Common:1; Rare:76 | ||||
chr1:95117559-95117714 | Rare:41 | ||||
chr1:95117997-95118146 | Rare:33 | ||||
chr1:95233908-95234352 | Common:6; Rare:137 | ||||
chr1:95234392-95234444 | Common:1; Rare:14 | ||||
chr1:96721524-96721612 | Common:1; Rare:33 | ||||
chr1:96721615-96721619 | Common:1; Rare:1 | ||||
chr1:96721648-96721870 | Common:1; Rare:98 | ||||
chr1:96721896-96722137 | Rare:77 | ||||
chr1:96722184-96722250 | Rare:12 |