Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93180281-93180764 | Common:2; Rare:194 | ||||
chr1:93345604-93345979 | Common:5; Rare:125 | ||||
chr1:93879123-93879293 | Common:2; Rare:64 | ||||
chr1:94541663-94541974 | Common:1; Rare:92 | ||||
chr1:94820154-94820357 | Common:4; Rare:47 | ||||
chr1:94926907-94927408 | Common:4; Rare:160 | ||||
chr1:95072865-95073023 | Common:1; Rare:60; Clinvar (benign):1 | ||||
chr1:95233959-95234236 | Common:5; Rare:84 | ||||
chr1:98661581-98661887 | Common:2; Rare:105 | ||||
chr1:99969922-99970145 | Common:2; Rare:61 | ||||
chr1:100132902-100133226 | Common:2; Rare:124 | ||||
chr1:100266109-100266352 | Common:2; Rare:84 | ||||
chr1:100894640-100894914 | Common:2; Rare:66 | ||||
chr1:100895982-100896147 | Rare:45 | ||||
chr1:101025682-101025910 | Common:2; Rare:62 |