Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109075933-109076252 | Rare:101 | ||||
chr1:109090697-109090860 | Common:2; Rare:39 | ||||
chr1:109090889-109091016 | Rare:35 | ||||
chr1:109656286-109656315 | Rare:7 | ||||
chr1:109984993-109985165 | Rare:63 | ||||
chr1:110339151-110339447 | Common:1; Rare:83 | ||||
chr1:110407597-110407809 | Common:2; Rare:92 | ||||
chr1:111140040-111140259 | Common:1; Rare:77 | ||||
chr1:112619607-112619851 | Common:1; Rare:81 | ||||
chr1:112956080-112956473 | Common:5; Rare:149; Clinvar:11; Clinvar (benign):3 | ||||
chr1:113904816-113905148 | Common:2; Rare:94; Clinvar (benign):1 | ||||
chr1:113929435-113929652 | Common:1; Rare:64 | ||||
chr1:114581607-114581815 | Rare:87 | ||||
chr1:114716701-114716985 | Common:4; Rare:110; Clinvar:5; Clinvar (benign):1 | ||||
chr1:117367306-117367516 | Common:5; Rare:78 |