Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92298888-92299076 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92785066-92785421 | Common:6; Rare:113 | ||||
chr1:92831871-92832139 | Common:1; Rare:117; Clinvar:7; Clinvar (benign):7 | ||||
chr1:93079018-93079308 | Common:3; Rare:123 | ||||
chr1:93179895-93179961 | Common:1; Rare:16 | ||||
chr1:93180070-93180762 | Common:2; Rare:272 | ||||
chr1:93345761-93345953 | Common:4; Rare:75 | ||||
chr1:93448012-93448252 | Common:2; Rare:81 | ||||
chr1:93879134-93879347 | Common:3; Rare:81 | ||||
chr1:94418215-94418470 | Common:2; Rare:90 | ||||
chr1:94926917-94927039 | Common:3; Rare:33 | ||||
chr1:94927048-94927446 | Common:1; Rare:132 | ||||
chr1:95072609-95072728 | Rare:32 | ||||
chr1:95072863-95073023 | Common:1; Rare:61; Clinvar (benign):1 | ||||
chr1:95116665-95116933 | Rare:45 |