Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1162626-1162948 | Common:2; Rare:111 | ||||
chr1:1163881-1163898 | Common:1; Rare:4 | ||||
chr1:1164592-1164856 | Common:1; Rare:92 | ||||
chr1:1347984-1348175 | Common:1; Rare:63 | ||||
chr1:1387542-1387804 | Common:3; Rare:89 | ||||
chr1:1527491-1527761 | Common:2; Rare:105 | ||||
chr1:1787018-1787150 | Rare:21 | ||||
chr1:2180281-2180295 | Rare:2 | ||||
chr1:2229223-2229499 | Rare:92; Clinvar:6; Clinvar (benign):8 | ||||
chr1:2229563-2229627 | Rare:23; Clinvar (benign):3 | ||||
chr1:2402864-2403108 | Rare:69 | ||||
chr1:2548872-2548971 | Common:3; Rare:28 | ||||
chr1:2578364-2578571 | Common:2; Rare:43 | ||||
chr1:3061848-3061952 | Rare:21 | ||||
chr1:3063035-3063274 | Rare:70 |