Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:195803298-195803479 | Common:1; Rare:32 | ||||
chr3:195809386-195809445 | Rare:12 | ||||
chr3:196502921-196503120 | Rare:74 | ||||
chr3:196966799-196966907 | Rare:20 | ||||
chr3:197454246-197454356 | Common:1; Rare:22 | ||||
chr3:197627810-197627968 | Common:5; Rare:47 | ||||
chr3:197850988-197851057 | Rare:10 | ||||
chr4:754156-754357 | Common:5; Rare:79 | ||||
chr4:868627-868829 | Common:1; Rare:69 | ||||
chr4:971645-971860 | Common:1; Rare:51 | ||||
chr4:1177776-1177798 | Rare:4 | ||||
chr4:1202230-1202506 | Common:2; Rare:58 | ||||
chr4:1805296-1805428 | Common:1; Rare:48; Clinvar (pathogenic):1 | ||||
chr4:1806073-1806326 | Common:2; Rare:95; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr4:1806661-1806840 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):2 |