Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:178094392-178094549 | Rare:69 | ||||
chr1:178725062-178725369 | Common:10; Rare:109 | ||||
chr1:178869214-178869329 | Common:1; Rare:18 | ||||
chr1:178871016-178871176 | Rare:28 | ||||
chr1:179081947-179082084 | Common:1; Rare:41 | ||||
chr1:179882123-179882398 | Common:1; Rare:52 | ||||
chr1:179882474-179882924 | Rare:220; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179882937-179883003 | Common:1; Rare:32; Clinvar:2; Clinvar (benign):2 | ||||
chr1:179883007-179883153 | Common:3; Rare:57 | ||||
chr1:179954679-179955005 | Common:1; Rare:70 | ||||
chr1:180154564-180155061 | Common:6; Rare:155 | ||||
chr1:180912556-180912867 | Common:1; Rare:73 | ||||
chr1:180940877-180941126 | Common:8; Rare:78 | ||||
chr1:181088494-181088752 | Common:1; Rare:98 | ||||
chr1:182388774-182389092 | Common:3; Rare:68 |