Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10694449-10694970 | Common:4; Rare:268 | ||||
chr1:10796554-10796954 | Common:6; Rare:194 | ||||
chr1:11012241-11012352 | Rare:26 | ||||
chr1:11059980-11060201 | Common:2; Rare:58 | ||||
chr1:11099817-11100037 | Common:2; Rare:82 | ||||
chr1:11262528-11262915 | Common:2; Rare:108 | ||||
chr1:11272873-11273272 | Common:1; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11273291-11273718 | Common:4; Rare:266; Clinvar:7; Clinvar (benign):4 | ||||
chr1:11654330-11654710 | Rare:97 | ||||
chr1:11655719-11656119 | Common:2; Rare:158 | ||||
chr1:11681050-11681490 | Common:4; Rare:131 | ||||
chr1:11681502-11681753 | Common:2; Rare:61 | ||||
chr1:11691448-11691597 | Common:2; Rare:37 | ||||
chr1:11735860-11736270 | Common:3; Rare:114 | ||||
chr1:11803525-11803828 | Rare:63 |