Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154956085-154956229 | Rare:40 | ||||
chr1:154961483-154961549 | Rare:21 | ||||
chr1:154965631-154965964 | Common:3; Rare:107 | ||||
chr1:154970703-154970908 | Common:1; Rare:44 | ||||
chr1:154974303-154974730 | Rare:107 | ||||
chr1:154983076-154983392 | Common:2; Rare:63; Clinvar (benign):1 | ||||
chr1:155135687-155135944 | Common:4; Rare:108 | ||||
chr1:155173113-155173409 | Common:3; Rare:118 | ||||
chr1:155173824-155173895 | Rare:13 | ||||
chr1:155174346-155174594 | Rare:57 | ||||
chr1:155207898-155208042 | Rare:36 | ||||
chr1:155209131-155209285 | Rare:69 | ||||
chr1:155244657-155244958 | Common:3; Rare:83 | ||||
chr1:155255434-155255560 | Common:1; Rare:27 | ||||
chr1:155308523-155308896 | Common:1; Rare:82 |