Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156601427-156601730 | Common:3; Rare:83 | ||||
chr1:156728394-156728469 | Rare:15 | ||||
chr1:156741071-156741417 | Common:1; Rare:91 | ||||
chr1:156767403-156767556 | Rare:48 | ||||
chr1:157138342-157138686 | Common:4; Rare:108 | ||||
chr1:159923730-159923887 | Common:1; Rare:27 | ||||
chr1:159924578-159924797 | Rare:46 | ||||
chr1:160343156-160343415 | Rare:102 | ||||
chr1:161021118-161021441 | Rare:77 | ||||
chr1:161045888-161046050 | Common:1; Rare:43 | ||||
chr1:161118019-161118146 | Rare:64 | ||||
chr1:161132411-161132709 | Common:1; Rare:95 | ||||
chr1:161166262-161166486 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
chr1:161199053-161199354 | Rare:47 | ||||
chr1:161314265-161314417 | Common:3; Rare:60; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 |