Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112956169-112956626 | Common:6; Rare:158; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073039-113073230 | Common:1; Rare:70 | ||||
chr1:113390180-113390523 | Common:1; Rare:83 | ||||
chr1:113759448-113759591 | Common:2; Rare:43 | ||||
chr1:113812251-113812544 | Common:2; Rare:123 | ||||
chr1:113904775-113905013 | Common:2; Rare:68; Clinvar (benign):2 | ||||
chr1:113905026-113905442 | Common:5; Rare:114 | ||||
chr1:117060203-117060360 | Common:2; Rare:47 | ||||
chr1:117929560-117929800 | Common:2; Rare:70 | ||||
chr1:119140640-119140730 | Rare:23 | ||||
chr1:119648138-119648358 | Common:3; Rare:79 | ||||
chr1:120176343-120176590 | Rare:55 | ||||
chr1:121184887-121185077 | Rare:69 | ||||
chr1:145823912-145824268 | Rare:127 | ||||
chr1:145845476-145845668 | Common:3; Rare:50 |