Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228109239-228109454 | Rare:71 | ||||
chr1:228139856-228140109 | Common:2; Rare:61 | ||||
chr1:228207901-228208075 | Common:1; Rare:39 | ||||
chr1:228277636-228277857 | Common:3; Rare:98 | ||||
chr1:228457860-228458113 | Common:1; Rare:81 | ||||
chr1:229271003-229271331 | Rare:108 | ||||
chr1:229508267-229508440 | Common:1; Rare:70 | ||||
chr1:229625958-229626261 | Rare:99 | ||||
chr1:230978753-230979144 | Common:2; Rare:154 | ||||
chr1:231241112-231241238 | Rare:65; Clinvar:2 | ||||
chr1:231337830-231338056 | Common:2; Rare:82 | ||||
chr1:231528519-231528728 | Common:2; Rare:77 | ||||
chr1:232805190-232805440 | Common:4; Rare:135 | ||||
chr1:233613325-233613843 | Common:3; Rare:123 | ||||
chr1:234373391-234373554 | Common:1; Rare:84; Clinvar (benign):3 |