Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:85276297-85276681 | Common:6; Rare:129; Clinvar (benign):3 | ||||
chr1:85708288-85708543 | Common:2; Rare:95 | ||||
chr1:86704460-86704613 | Rare:57 | ||||
chr1:86704700-86704939 | Common:3; Rare:88 | ||||
chr1:86914323-86914755 | Common:1; Rare:129 | ||||
chr1:88683980-88684445 | Common:3; Rare:129 | ||||
chr1:88684497-88684628 | Rare:31 | ||||
chr1:88992583-88992976 | Common:3; Rare:101 | ||||
chr1:89198845-89199001 | Common:1; Rare:26 | ||||
chr1:89363774-89364150 | Rare:58 | ||||
chr1:89632887-89633190 | Common:1; Rare:83 | ||||
chr1:89820911-89821202 | Common:1; Rare:89 | ||||
chr1:89994977-89995218 | Common:2; Rare:89 | ||||
chr1:91500750-91500901 | Common:2; Rare:49 | ||||
chr1:91885948-91886352 | Rare:165 |