Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:91880677-91880823 | Common:2; Rare:39 | ||||
chr7:91940831-91940989 | Common:3; Rare:53; Clinvar:3; Clinvar (benign):1 | ||||
chr7:92134360-92134594 | Rare:73 | ||||
chr7:92245865-92245974 | Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
chr7:92528389-92528808 | Common:3; Rare:130; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr7:92833926-92834080 | Rare:37 | ||||
chr7:93232189-93232385 | Common:2; Rare:38 | ||||
chr7:94004317-94004472 | Rare:46 | ||||
chr7:94656100-94656381 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
chr7:95396354-95396472 | Common:2; Rare:49 | ||||
chr7:95434899-95435097 | Common:1; Rare:88; Clinvar (benign):1 | ||||
chr7:95587364-95587469 | Common:1; Rare:29 | ||||
chr7:95592576-95592880 | Common:2; Rare:87 | ||||
chr7:95596096-95596237 | Rare:52 | ||||
chr7:95596240-95596380 | Rare:49 |