Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:74657380-74657722 | Common:2; Rare:106 | ||||
chr7:75611763-75611908 | Common:1; Rare:28 | ||||
chr7:75914925-75915164 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
chr7:75994512-75994749 | Common:3; Rare:119 | ||||
chr7:76047872-76048220 | Common:3; Rare:118 | ||||
chr7:76302842-76303075 | Rare:98; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr7:76303608-76303864 | Common:1; Rare:113; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
chr7:77696236-77696465 | Rare:91 | ||||
chr7:77696735-77696882 | Rare:66 | ||||
chr7:77798344-77798910 | Common:1; Rare:137 | ||||
chr7:79453548-79454126 | Common:3; Rare:142 | ||||
chr7:87152301-87152480 | Common:1; Rare:58 | ||||
chr7:87219662-87219851 | Rare:55 | ||||
chr7:87345437-87345722 | Common:5; Rare:89 | ||||
chr7:87876243-87876715 | Common:3; Rare:205 |