Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:86704482-86704627 | Rare:51 | ||||
chr1:86704719-86704966 | Common:3; Rare:87 | ||||
chr1:86914339-86914787 | Common:1; Rare:141 | ||||
chr1:87328549-87328951 | Common:3; Rare:151 | ||||
chr1:87329010-87329173 | Common:2; Rare:41 | ||||
chr1:88683943-88684413 | Common:4; Rare:131 | ||||
chr1:88992593-88993123 | Common:6; Rare:132 | ||||
chr1:89065169-89065440 | Common:2; Rare:42 | ||||
chr1:89632900-89633175 | Common:1; Rare:78 | ||||
chr1:89994981-89995218 | Common:2; Rare:89 | ||||
chr1:91886106-91886377 | Rare:105 | ||||
chr1:92298919-92299064 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92831924-92832112 | Common:1; Rare:91; Clinvar:6; Clinvar (benign):5 | ||||
chr1:93079056-93079310 | Common:3; Rare:109 | ||||
chr1:93180055-93180251 | Rare:71 |