Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91022601-91022645 | Rare:11 | ||||
chr1:91022692-91022737 | Rare:7 | ||||
chr1:91500673-91500919 | Common:2; Rare:78 | ||||
chr1:91501016-91501210 | Rare:62 | ||||
chr1:91501268-91501528 | Rare:64 | ||||
chr1:91886112-91886348 | Rare:97 | ||||
chr1:92080208-92080381 | Common:1; Rare:36 | ||||
chr1:92080405-92080589 | Common:2; Rare:56 | ||||
chr1:92298603-92299140 | Common:2; Rare:181; Clinvar:2; Clinvar (benign):2 | ||||
chr1:92483674-92483929 | Common:2; Rare:53 | ||||
chr1:92483936-92484188 | Rare:43 | ||||
chr1:92484526-92485185 | Common:5; Rare:121 | ||||
chr1:92485188-92485596 | Common:3; Rare:91 | ||||
chr1:92485852-92486306 | Common:1; Rare:101 | ||||
chr1:92486833-92487082 | Common:2; Rare:66; Clinvar (benign):1 |