Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:84690425-84690688 | Rare:82 | ||||
chr1:84997063-84997234 | Common:8; Rare:51 | ||||
chr1:85276112-85276306 | Common:3; Rare:48 | ||||
chr1:85276341-85276774 | Common:5; Rare:135; Clinvar (benign):1 | ||||
chr1:85708280-85708506 | Common:2; Rare:81 | ||||
chr1:86395987-86396103 | Common:1; Rare:36 | ||||
chr1:86396238-86396435 | Common:3; Rare:49 | ||||
chr1:86704473-86704632 | Rare:58 | ||||
chr1:86704682-86705086 | Common:4; Rare:133 | ||||
chr1:86914323-86914760 | Common:1; Rare:132 | ||||
chr1:87331588-87331753 | Rare:49 | ||||
chr1:88684064-88684396 | Common:3; Rare:85 | ||||
chr1:88684497-88684583 | Rare:18 | ||||
chr1:88992591-88992988 | Common:3; Rare:102 | ||||
chr1:89022721-89022940 | Rare:35 |