Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:633706-634015 | Common:7; Rare:110 | ||||
chr1:778607-778820 | Common:3; Rare:90 | ||||
chr1:827465-827679 | Common:2; Rare:87 | ||||
chr1:1387555-1387804 | Common:3; Rare:82 | ||||
chr1:1403134-1403196 | Rare:15 | ||||
chr1:3410587-3410614 | Rare:3 | ||||
chr1:9151689-9151855 | Rare:54 | ||||
chr1:9730679-9730750 | Rare:28 | ||||
chr1:11069760-11069930 | Common:1; Rare:31 | ||||
chr1:11071020-11071047 | Rare:9 | ||||
chr1:11204675-11204980 | Common:1; Rare:61 | ||||
chr1:12585054-12585320 | Common:10; Rare:59 | ||||
chr1:12619043-12619221 | Rare:33 | ||||
chr1:14256182-14256394 | Common:1; Rare:36 | ||||
chr1:15725070-15725483 | Common:3; Rare:130; Clinvar (benign):2 |