Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179293628-179293916 | Common:3; Rare:95 | ||||
chr1:179877766-179877896 | Rare:27 | ||||
chr1:179882155-179882318 | Common:1; Rare:32 | ||||
chr1:179882458-179882901 | Rare:214; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179882986-179883153 | Common:3; Rare:65; Clinvar (benign):1 | ||||
chr1:179954686-179954827 | Rare:29 | ||||
chr1:180154668-180154896 | Common:3; Rare:78 | ||||
chr1:180502265-180502647 | Common:1; Rare:134 | ||||
chr1:180502805-180502998 | Rare:71 | ||||
chr1:180631841-180632200 | Common:5; Rare:131 | ||||
chr1:181033709-181034028 | Common:1; Rare:72 | ||||
chr1:181088512-181088704 | Rare:64 | ||||
chr1:182391303-182391489 | Rare:40 | ||||
chr1:182589203-182589286 | Rare:19 | ||||
chr1:182604367-182604583 | Rare:47 |