Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156282786-156283036 | Common:2; Rare:59 | ||||
chr1:156338152-156338577 | Common:2; Rare:156 | ||||
chr1:156591678-156591986 | Common:5; Rare:139; Clinvar (pathogenic):1 | ||||
chr1:156601410-156601696 | Common:2; Rare:84 | ||||
chr1:156642029-156642177 | Rare:41 | ||||
chr1:156728383-156728489 | Common:1; Rare:22 | ||||
chr1:156728581-156728899 | Rare:91 | ||||
chr1:156729079-156729155 | Rare:32 | ||||
chr1:156741029-156741379 | Rare:94 | ||||
chr1:156751843-156751975 | Rare:39 | ||||
chr1:156766884-156767208 | Rare:55 | ||||
chr1:156767393-156767574 | Rare:60 | ||||
chr1:157138342-157138659 | Common:3; Rare:96 | ||||
chr1:158999741-159000081 | Common:2; Rare:71 | ||||
chr1:159780727-159781042 | Common:5; Rare:73 |