Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:108692189-108692338 | Common:1; Rare:53 | ||||
chr1:109548505-109548732 | Common:4; Rare:86 | ||||
chr1:109619687-109619858 | Rare:37 | ||||
chr1:110339154-110339447 | Common:1; Rare:82 | ||||
chr1:110407632-110407798 | Common:2; Rare:78 | ||||
chr1:111140050-111140286 | Common:2; Rare:79 | ||||
chr1:112395954-112396281 | Common:2; Rare:105 | ||||
chr1:112619109-112619190 | Rare:30 | ||||
chr1:112619690-112619883 | Common:2; Rare:70 | ||||
chr1:112956178-112956467 | Common:5; Rare:126; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073105-113073206 | Rare:39 | ||||
chr1:113905221-113905407 | Common:3; Rare:51 | ||||
chr1:114716722-114716862 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):1 | ||||
chr1:117929568-117929795 | Common:1; Rare:68 | ||||
chr1:119140634-119140705 | Rare:26 |