Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:76302839-76303075 | Rare:100; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr7:77537320-77537590 | Rare:80 | ||||
chr7:77696133-77696467 | Common:1; Rare:124 | ||||
chr7:77697007-77697159 | Common:1; Rare:53 | ||||
chr7:77798344-77798956 | Common:1; Rare:146 | ||||
chr7:79453552-79453770 | Common:1; Rare:54 | ||||
chr7:79453795-79454123 | Common:2; Rare:79 | ||||
chr7:84194962-84195129 | Common:5; Rare:37 | ||||
chr7:87152309-87152474 | Common:1; Rare:54 | ||||
chr7:87152543-87152687 | Rare:42 | ||||
chr7:87345412-87345701 | Common:4; Rare:90 | ||||
chr7:87876342-87876653 | Common:1; Rare:135 | ||||
chr7:90211633-90211890 | Common:3; Rare:78 | ||||
chr7:90245099-90245226 | Rare:41 | ||||
chr7:90346573-90346736 | Common:3; Rare:69 |