Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52366388-52366574 | Common:3; Rare:61 | ||||
chr1:52404101-52404188 | Rare:14 | ||||
chr1:52404345-52404676 | Common:1; Rare:91 | ||||
chr1:52552646-52552726 | Rare:14 | ||||
chr1:52552913-52553116 | Rare:67 | ||||
chr1:52553373-52553699 | Common:3; Rare:88 | ||||
chr1:52602316-52602424 | Common:2; Rare:39 | ||||
chr1:52602466-52602550 | Rare:23 | ||||
chr1:52633016-52633174 | Common:1; Rare:34 | ||||
chr1:52698045-52698162 | Rare:24 | ||||
chr1:52698237-52698539 | Common:3; Rare:97; Clinvar (pathogenic):1 | ||||
chr1:52726292-52726572 | Common:9; Rare:112 | ||||
chr1:52842548-52842972 | Common:8; Rare:140 | ||||
chr1:52843045-52843254 | Common:4; Rare:55 | ||||
chr1:52921482-52921555 | Common:1; Rare:30 |