Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:175006892-175007152 | Common:2; Rare:44 | ||||
chr1:176207224-176207344 | Common:1; Rare:62 | ||||
chr1:178094387-178094475 | Rare:39 | ||||
chr1:178724980-178725344 | Common:11; Rare:117 | ||||
chr1:178869184-178869477 | Common:1; Rare:44 | ||||
chr1:178870991-178871056 | Rare:13 | ||||
chr1:178871059-178871217 | Rare:32 | ||||
chr1:179081894-179082086 | Common:1; Rare:59 | ||||
chr1:179143047-179143243 | Rare:35 | ||||
chr1:179293614-179293934 | Common:3; Rare:100 | ||||
chr1:179882062-179882358 | Common:1; Rare:67 | ||||
chr1:179882409-179882971 | Common:1; Rare:261; Clinvar:11; Clinvar (benign):4 | ||||
chr1:179954578-179954834 | Common:1; Rare:60 | ||||
chr1:179954979-179955008 | Rare:7 | ||||
chr1:180154725-180154906 | Common:1; Rare:74 |