Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92784661-92784896 | Common:1; Rare:58 | ||||
chr1:92785018-92785304 | Common:4; Rare:109 | ||||
chr1:92831850-92832139 | Common:1; Rare:124; Clinvar:7; Clinvar (benign):7 | ||||
chr1:92832246-92832477 | Rare:74 | ||||
chr1:92961055-92961402 | Common:2; Rare:88 | ||||
chr1:92961405-92961899 | Common:4; Rare:149 | ||||
chr1:93079011-93079393 | Common:4; Rare:151 | ||||
chr1:93079468-93079543 | Rare:16 | ||||
chr1:93179679-93179837 | Rare:27 | ||||
chr1:93179859-93180048 | Common:1; Rare:51 | ||||
chr1:93180252-93180829 | Common:2; Rare:234 | ||||
chr1:93181080-93181295 | Common:1; Rare:36 | ||||
chr1:93345188-93345436 | Common:2; Rare:41 | ||||
chr1:93345673-93346016 | Common:6; Rare:122 | ||||
chr1:93346255-93346422 | Common:1; Rare:37 |