Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:44107915-44108084 | Common:2; Rare:59; Clinvar (pathogenic):1 | ||||
chr7:44113248-44113655 | Common:1; Rare:115 | ||||
chr7:44467654-44467852 | Common:2; Rare:30 | ||||
chr7:44830911-44830986 | Rare:11 | ||||
chr7:44986592-44986758 | Common:2; Rare:86 | ||||
chr7:45768916-45769091 | Rare:50 | ||||
chr7:55083420-55083489 | Rare:13 | ||||
chr7:55151225-55151354 | Rare:27 | ||||
chr7:65750910-65751129 | Common:3; Rare:96 | ||||
chr7:66493543-66493737 | Common:3; Rare:80 | ||||
chr7:66654282-66654567 | Common:2; Rare:90 | ||||
chr7:66844892-66845061 | Common:2; Rare:70 | ||||
chr7:67302400-67302692 | Common:5; Rare:94 | ||||
chr7:72829321-72829505 | Rare:51 | ||||
chr7:73005862-73006140 | Rare:29 |