Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:84479509-84479573 | Rare:28 | ||||
chr1:84690425-84690706 | Rare:91 | ||||
chr1:85276341-85276774 | Common:5; Rare:135; Clinvar (benign):1 | ||||
chr1:85708049-85708498 | Common:4; Rare:147 | ||||
chr1:86395977-86396085 | Common:1; Rare:35 | ||||
chr1:86396259-86396430 | Common:3; Rare:44 | ||||
chr1:86704460-86704632 | Rare:65 | ||||
chr1:86704719-86704932 | Common:3; Rare:79 | ||||
chr1:86914323-86914787 | Common:1; Rare:144 | ||||
chr1:87331543-87331769 | Common:1; Rare:70 | ||||
chr1:88684064-88684355 | Common:3; Rare:79 | ||||
chr1:88891485-88891675 | Common:1; Rare:89 | ||||
chr1:88891677-88891740 | Rare:16 | ||||
chr1:88992605-88992982 | Common:3; Rare:96 | ||||
chr1:89065203-89065395 | Rare:28 |