Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93079031-93079348 | Common:4; Rare:134 | ||||
chr1:93179902-93179922 | Rare:3 | ||||
chr1:93180377-93180754 | Common:2; Rare:161 | ||||
chr1:93345757-93346098 | Common:5; Rare:126 | ||||
chr1:93447996-93448415 | Common:3; Rare:130 | ||||
chr1:93448661-93448858 | Common:3; Rare:61 | ||||
chr1:93846609-93846781 | Common:1; Rare:56 | ||||
chr1:93847459-93847500 | Rare:13 | ||||
chr1:93879097-93879358 | Common:3; Rare:99 | ||||
chr1:94237566-94237728 | Rare:65 | ||||
chr1:94418108-94418481 | Common:3; Rare:137 | ||||
chr1:94927048-94927456 | Common:1; Rare:135 | ||||
chr1:95072863-95073018 | Common:1; Rare:61; Clinvar (benign):1 | ||||
chr1:95233973-95234236 | Common:5; Rare:81 | ||||
chr1:96721579-96722069 | Common:2; Rare:213 |