Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:95207406-95207604 | Rare:79 | ||||
chr2:95402607-95402777 | Rare:55 | ||||
chr2:96208252-96208427 | Rare:86 | ||||
chr2:96208793-96208950 | Common:3; Rare:63 | ||||
chr2:96265959-96266348 | Common:2; Rare:118; Clinvar:1 | ||||
chr2:97094826-97094966 | Common:1; Rare:29 | ||||
chr2:97645780-97646156 | Common:3; Rare:112 | ||||
chr2:97663924-97664267 | Common:1; Rare:105 | ||||
chr2:98086999-98087195 | Rare:51 | ||||
chr2:98608386-98608649 | Common:1; Rare:114; Clinvar (benign):1 | ||||
chr2:98731056-98731308 | Common:3; Rare:88 | ||||
chr2:99141123-99141445 | Common:1; Rare:118 | ||||
chr2:99141506-99141766 | Common:2; Rare:90 | ||||
chr2:99154877-99155101 | Common:2; Rare:90; Clinvar (benign):3 | ||||
chr2:99180979-99181226 | Common:2; Rare:72 |