Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93449142-93449397 | Common:1; Rare:74 | ||||
chr1:93591832-93592016 | Rare:28 | ||||
chr1:93592393-93592679 | Common:1; Rare:54 | ||||
chr1:93617665-93617889 | Common:3; Rare:41 | ||||
chr1:93638501-93638768 | Common:1; Rare:51 | ||||
chr1:93639123-93639245 | Common:2; Rare:27 | ||||
chr1:93828487-93828622 | Rare:26 | ||||
chr1:93846241-93846446 | Common:1; Rare:66 | ||||
chr1:93848080-93848259 | Common:2; Rare:48 | ||||
chr1:94045572-94045895 | Common:3; Rare:76; Clinvar (benign):1 | ||||
chr1:94061975-94062396 | Rare:72 | ||||
chr1:94069089-94069178 | Rare:14 | ||||
chr1:94090980-94091073 | Common:1; Rare:21 | ||||
chr1:94105516-94105855 | Common:1; Rare:57 | ||||
chr1:94246517-94246749 | Common:1; Rare:42 |