Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89198922-89198977 | Rare:7 | ||||
chr1:89994977-89995178 | Common:2; Rare:75 | ||||
chr1:91021978-91022141 | Rare:50 | ||||
chr1:91500631-91500909 | Common:2; Rare:78 | ||||
chr1:92029890-92030010 | Rare:34 | ||||
chr1:92298927-92299074 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
chr1:93079056-93079290 | Common:3; Rare:103 | ||||
chr1:93180355-93180736 | Common:1; Rare:166 | ||||
chr1:93345788-93345912 | Common:3; Rare:50 | ||||
chr1:93879097-93879293 | Common:2; Rare:76 | ||||
chr1:94418119-94418464 | Common:2; Rare:122 | ||||
chr1:94541730-94541991 | Rare:76 | ||||
chr1:94820264-94820382 | Common:2; Rare:33 | ||||
chr1:94927049-94927467 | Common:1; Rare:138 | ||||
chr1:95072872-95073018 | Rare:56 |