Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112619748-112619851 | Common:1; Rare:40 | ||||
chr1:112956141-112956437 | Common:4; Rare:126; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073085-113073221 | Common:1; Rare:46 | ||||
chr1:113905032-113905387 | Common:5; Rare:99 | ||||
chr1:115089462-115089587 | Common:1; Rare:50 | ||||
chr1:115641790-115642027 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
chr1:115768537-115768965 | Common:8; Rare:90; Clinvar:7; Clinvar (benign):5 | ||||
chr1:116373109-116373439 | Common:1; Rare:108 | ||||
chr1:116570968-116571197 | Common:2; Rare:66 | ||||
chr1:116909584-116910230 | Common:4; Rare:189 | ||||
chr1:117060203-117060341 | Common:2; Rare:35 | ||||
chr1:117121714-117121988 | Common:1; Rare:84 | ||||
chr1:117929560-117929787 | Common:1; Rare:67 | ||||
chr1:119140628-119140781 | Common:1; Rare:51 | ||||
chr1:119648120-119648333 | Common:3; Rare:77 |