Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9423433-9423697 | Rare:85 | ||||
chr2:9555712-9555943 | Common:2; Rare:80 | ||||
chr2:9843251-9843512 | Common:6; Rare:73 | ||||
chr2:10302731-10302991 | Common:4; Rare:79 | ||||
chr2:10448306-10448731 | Common:1; Rare:134 | ||||
chr2:17753746-17753867 | Common:1; Rare:45 | ||||
chr2:23940370-23940518 | Common:3; Rare:54 | ||||
chr2:24076335-24076552 | Rare:56 | ||||
chr2:24123352-24123510 | Common:1; Rare:39 | ||||
chr2:24793140-24793453 | Rare:138; Clinvar:1 | ||||
chr2:24971902-24972136 | Common:1; Rare:77 | ||||
chr2:26244602-26244943 | Common:2; Rare:123; Clinvar:5; Clinvar (benign):6 | ||||
chr2:26345809-26346181 | Common:1; Rare:110 | ||||
chr2:27032844-27033078 | Rare:84 | ||||
chr2:27078529-27079017 | Common:4; Rare:123 |