Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112619099-112619236 | Rare:49 | ||||
chr1:112619675-112619847 | Common:1; Rare:62 | ||||
chr1:112956180-112956473 | Common:5; Rare:129; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073085-113073238 | Common:1; Rare:55 | ||||
chr1:113812264-113812587 | Common:2; Rare:127 | ||||
chr1:113904824-113905387 | Common:7; Rare:169; Clinvar (benign):1 | ||||
chr1:113979296-113979519 | Rare:55 | ||||
chr1:114581578-114581846 | Common:1; Rare:116 | ||||
chr1:114716722-114716876 | Common:1; Rare:72; Clinvar:4; Clinvar (benign):1 | ||||
chr1:114757931-114758118 | Common:3; Rare:63 | ||||
chr1:114780539-114780796 | Common:1; Rare:101 | ||||
chr1:116570970-116571195 | Common:2; Rare:66 | ||||
chr1:117060056-117060363 | Common:6; Rare:83 | ||||
chr1:117121726-117122002 | Common:1; Rare:81 | ||||
chr1:117929516-117929800 | Common:2; Rare:82 |