Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:10939827-10939860 | Rare:11 | ||||
chr7:10940048-10940595 | Common:6; Rare:213; Clinvar (benign):3 | ||||
chr7:10973722-10973941 | Rare:96 | ||||
chr7:11832225-11832369 | Common:1; Rare:38 | ||||
chr7:11832430-11832508 | Rare:12 | ||||
chr7:12210936-12211395 | Common:5; Rare:172 | ||||
chr7:12686736-12686908 | Common:2; Rare:52 | ||||
chr7:16645511-16646280 | Common:6; Rare:275 | ||||
chr7:16753443-16753535 | Rare:22 | ||||
chr7:16753611-16753959 | Common:2; Rare:124 | ||||
chr7:17940389-17940624 | Common:2; Rare:115 | ||||
chr7:19773329-19773710 | Common:2; Rare:95 | ||||
chr7:20330631-20331116 | Common:2; Rare:129 | ||||
chr7:20786805-20787135 | Common:2; Rare:96 | ||||
chr7:21427262-21427544 | Common:4; Rare:101 |