Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169367784-169368254 | Common:3; Rare:87 | ||||
chr1:169427418-169427503 | Rare:16 | ||||
chr1:169485694-169486169 | Common:1; Rare:143; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794884-169795094 | Common:3; Rare:55 | ||||
chr1:169893649-169893730 | Common:1; Rare:26 | ||||
chr1:169894263-169894394 | Common:2; Rare:42 | ||||
chr1:170074465-170074756 | Common:2; Rare:90 | ||||
chr1:170532033-170532404 | Common:4; Rare:142; Clinvar:2 | ||||
chr1:171741908-171742347 | Common:4; Rare:124 | ||||
chr1:171781555-171781708 | Common:1; Rare:35 | ||||
chr1:173476912-173477492 | Common:6; Rare:186 | ||||
chr1:173714861-173715078 | Common:1; Rare:49 | ||||
chr1:173824390-173824714 | Rare:59; Clinvar:2 | ||||
chr1:173824817-173824985 | Rare:40 | ||||
chr1:173867969-173868385 | Common:2; Rare:140 |