Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:3900180-3900406 | Common:12; Rare:114 | ||||
chr1:6208680-6208860 | Common:1; Rare:49 | ||||
chr1:7771061-7771363 | Common:4; Rare:110 | ||||
chr1:7961419-7961780 | Common:4; Rare:126; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878578-8878857 | Rare:145 | ||||
chr1:9943258-9943488 | Common:3; Rare:60 | ||||
chr1:10032684-10032968 | Common:2; Rare:77 | ||||
chr1:10398868-10399120 | Common:2; Rare:100 | ||||
chr1:11262484-11262817 | Common:2; Rare:104 | ||||
chr1:11272922-11273223 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11654396-11654493 | Rare:27 | ||||
chr1:11654710-11654931 | Common:4; Rare:59 | ||||
chr1:11691477-11691855 | Common:4; Rare:83 | ||||
chr1:11805935-11806265 | Common:2; Rare:89; Clinvar:1 | ||||
chr1:12019243-12019533 | Common:5; Rare:100 |