Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6208680-6208865 | Common:1; Rare:50 | ||||
chr1:6358927-6359115 | Rare:35 | ||||
chr1:6419913-6420023 | Rare:32 | ||||
chr1:6579781-6580038 | Common:4; Rare:82 | ||||
chr1:8878578-8878905 | Rare:174 | ||||
chr1:9687529-9687680 | Common:1; Rare:37 | ||||
chr1:9942982-9943010 | Common:1; Rare:7 | ||||
chr1:9943247-9943489 | Common:3; Rare:62 | ||||
chr1:11262493-11262817 | Common:2; Rare:98 | ||||
chr1:11273419-11273510 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11654831-11654909 | Common:1; Rare:20 | ||||
chr1:11805935-11806252 | Common:2; Rare:85; Clinvar:1 | ||||
chr1:11934486-11934754 | Common:5; Rare:88; Clinvar:5; Clinvar (benign):1 | ||||
chr1:12618189-12618475 | Common:2; Rare:61 | ||||
chr1:13749193-13749451 | Common:2; Rare:92 |