Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:108692231-108692353 | Rare:40 | ||||
chr1:109548507-109548692 | Common:4; Rare:67 | ||||
chr1:109687739-109687846 | Common:2; Rare:13 | ||||
chr1:110339154-110339440 | Common:1; Rare:79 | ||||
chr1:110407624-110407795 | Common:2; Rare:79 | ||||
chr1:111140050-111140269 | Common:1; Rare:77 | ||||
chr1:112619117-112619193 | Rare:28 | ||||
chr1:112619612-112619851 | Common:1; Rare:80 | ||||
chr1:112956180-112956461 | Common:5; Rare:124; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073081-113073206 | Rare:43 | ||||
chr1:114670047-114670255 | Common:1; Rare:61 | ||||
chr1:114780628-114780748 | Rare:38 | ||||
chr1:117929591-117929795 | Rare:56 | ||||
chr1:119140645-119140724 | Rare:22 | ||||
chr1:145823937-145824205 | Rare:93 |