Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:77682638-77682707 | Rare:19 | ||||
chr1:77888078-77888355 | Common:1; Rare:66 | ||||
chr1:77888373-77888758 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77979006-77979291 | Common:2; Rare:101 | ||||
chr1:77979468-77979536 | Common:1; Rare:19 | ||||
chr1:78004550-78004960 | Common:4; Rare:95 | ||||
chr1:84077908-84078141 | Common:1; Rare:89 | ||||
chr1:84479202-84479313 | Common:3; Rare:57 | ||||
chr1:84574413-84574553 | Common:1; Rare:44 | ||||
chr1:84690425-84690706 | Rare:91 | ||||
chr1:85276484-85276774 | Common:3; Rare:89 | ||||
chr1:85708304-85708506 | Common:2; Rare:71 | ||||
chr1:86704457-86704651 | Rare:76 | ||||
chr1:86704704-86704971 | Common:3; Rare:95 | ||||
chr1:86914323-86914684 | Common:1; Rare:99 |