Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109619697-109619908 | Rare:46 | ||||
chr1:109656243-109656362 | Rare:29 | ||||
chr1:109667921-109668101 | Common:1; Rare:53 | ||||
chr1:110339156-110339461 | Common:1; Rare:88 | ||||
chr1:110407616-110407805 | Common:2; Rare:88 | ||||
chr1:111139788-111139860 | Rare:12 | ||||
chr1:111140049-111140292 | Common:2; Rare:82 | ||||
chr1:111619590-111619847 | Common:2; Rare:89 | ||||
chr1:112395980-112396262 | Common:1; Rare:88 | ||||
chr1:112619101-112619236 | Rare:49 | ||||
chr1:112619642-112619877 | Common:2; Rare:84 | ||||
chr1:112674549-112674922 | Common:1; Rare:81 | ||||
chr1:112707080-112707252 | Rare:62 | ||||
chr1:112956150-112956481 | Common:5; Rare:139; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073085-113073238 | Common:1; Rare:55 |