Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:66996575-66996896 | Common:2; Rare:67 | ||||
chr7:73522248-73522418 | Common:1; Rare:55 | ||||
chr7:73683419-73683642 | Common:3; Rare:95 | ||||
chr7:74254366-74254520 | Rare:70 | ||||
chr7:74289284-74289434 | Common:3; Rare:57 | ||||
chr7:76047783-76048194 | Common:3; Rare:123 | ||||
chr7:76302866-76303072 | Rare:87; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr7:77696207-77696467 | Rare:104 | ||||
chr7:77696782-77697050 | Rare:117 | ||||
chr7:77798320-77798977 | Common:1; Rare:153 | ||||
chr7:79453565-79453763 | Common:1; Rare:52 | ||||
chr7:79453838-79454121 | Common:1; Rare:72 | ||||
chr7:84194751-84194789 | Rare:2 | ||||
chr7:87152296-87152544 | Common:2; Rare:78 | ||||
chr7:87345461-87345743 | Common:6; Rare:88 |