Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109656191-109656255 | Rare:8 | ||||
chr1:109656272-109656374 | Rare:27 | ||||
chr1:110339149-110339466 | Common:1; Rare:93 | ||||
chr1:110407562-110407845 | Common:4; Rare:120 | ||||
chr1:111140036-111140269 | Common:1; Rare:84 | ||||
chr1:111739333-111739561 | Common:3; Rare:58 | ||||
chr1:112619109-112619205 | Rare:33 | ||||
chr1:112619739-112619851 | Common:1; Rare:42 | ||||
chr1:112956175-112956417 | Common:4; Rare:107; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073081-113073268 | Common:1; Rare:74 | ||||
chr1:113904835-113905344 | Common:5; Rare:151; Clinvar (benign):1 | ||||
chr1:114581572-114581830 | Common:1; Rare:116 | ||||
chr1:114780547-114780785 | Common:1; Rare:92 | ||||
chr1:115089453-115089622 | Common:3; Rare:64 | ||||
chr1:117060184-117060341 | Common:2; Rare:39 |