Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161766164-161766374 | Common:3; Rare:65 | ||||
chr1:162023625-162023679 | Rare:14 | ||||
chr1:165768778-165768904 | Common:1; Rare:56 | ||||
chr1:167935772-167936308 | Common:3; Rare:155 | ||||
chr1:167936550-167936999 | Common:1; Rare:159 | ||||
chr1:169367739-169368326 | Common:4; Rare:118 | ||||
chr1:169485941-169486114 | Rare:39; Clinvar:1 | ||||
chr1:173477153-173477492 | Common:4; Rare:122 | ||||
chr1:173824278-173824708 | Rare:88; Clinvar:1 | ||||
chr1:179081912-179082116 | Common:1; Rare:64 | ||||
chr1:179882523-179882853 | Rare:162; Clinvar:7; Clinvar (benign):2 | ||||
chr1:182391316-182391480 | Rare:33 | ||||
chr1:182839023-182839376 | Common:2; Rare:114 | ||||
chr1:183023079-183023314 | Common:4; Rare:58 | ||||
chr1:183635637-183636099 | Common:4; Rare:130 |