Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1630423-1630525 | Rare:42 | ||||
chr1:1781915-1782199 | Rare:63 | ||||
chr1:1858693-1858932 | Common:1; Rare:55 | ||||
chr1:1859333-1859448 | Rare:29 | ||||
chr1:1891633-1891685 | Common:1; Rare:9 | ||||
chr1:1908974-1909410 | Common:5; Rare:134 | ||||
chr1:1996291-1996410 | Rare:16 | ||||
chr1:2044905-2045084 | Common:1; Rare:45 | ||||
chr1:2174453-2174549 | Common:1; Rare:28 | ||||
chr1:2174677-2174701 | Rare:7 | ||||
chr1:2189477-2189744 | Common:2; Rare:104 | ||||
chr1:2189822-2190077 | Rare:66 | ||||
chr1:2205357-2205576 | Rare:63 | ||||
chr1:2227552-2228076 | Common:3; Rare:210 | ||||
chr1:2229434-2229551 | Rare:36; Clinvar (benign):3 |