Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:77888345-77888513 | Common:2; Rare:39 | ||||
chr1:77888516-77888718 | Rare:47; Clinvar:2 | ||||
chr1:77941958-77942109 | Rare:58; Clinvar:4; Clinvar (benign):2 | ||||
chr1:77978910-77979298 | Common:3; Rare:143 | ||||
chr1:77979468-77979547 | Common:1; Rare:24 | ||||
chr1:78004546-78005001 | Common:4; Rare:100 | ||||
chr1:79006665-79006933 | Common:1; Rare:86 | ||||
chr1:84077864-84078138 | Common:1; Rare:105 | ||||
chr1:84479202-84479290 | Common:2; Rare:43 | ||||
chr1:84574409-84574585 | Common:1; Rare:53 | ||||
chr1:84690425-84690688 | Rare:82 | ||||
chr1:84997079-84997225 | Common:6; Rare:42 | ||||
chr1:85062135-85062390 | Common:2; Rare:71 | ||||
chr1:85276378-85276774 | Common:5; Rare:121 | ||||
chr1:85708314-85708506 | Common:2; Rare:66 |