Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:27740069-27740199 | Common:5; Rare:31 | ||||
chr7:28180583-28180680 | Common:1; Rare:38 | ||||
chr7:29194074-29194459 | Rare:98 | ||||
chr7:29194719-29194938 | Common:2; Rare:54 | ||||
chr7:29563679-29563833 | Rare:42 | ||||
chr7:30504763-30505069 | Common:1; Rare:100 | ||||
chr7:30594722-30594952 | Common:3; Rare:109; Clinvar:6; Clinvar (benign):6 | ||||
chr7:30682430-30682604 | Rare:51 | ||||
chr7:30771302-30771470 | Common:1; Rare:55 | ||||
chr7:32495240-32495575 | Rare:86 | ||||
chr7:33040904-33041048 | Common:1; Rare:26 | ||||
chr7:33129234-33129578 | Common:5; Rare:96 | ||||
chr7:35694872-35695248 | Common:3; Rare:106 | ||||
chr7:35800721-35801054 | Common:1; Rare:115 | ||||
chr7:39566316-39566445 | Common:1; Rare:63 |