Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68956099-68956228 | Rare:59 | ||||
chr10:69087975-69088261 | Rare:64 | ||||
chr10:69179943-69180301 | Common:2; Rare:112 | ||||
chr10:69415930-69416429 | Common:3; Rare:158 | ||||
chr10:69416455-69417118 | Common:9; Rare:148 | ||||
chr10:69483341-69483552 | Common:2; Rare:36 | ||||
chr10:70132756-70132896 | Rare:41 | ||||
chr10:70233323-70233630 | Common:6; Rare:105; Clinvar (benign):1 | ||||
chr10:70403823-70404191 | Common:1; Rare:121 | ||||
chr10:70404268-70404435 | Rare:58 | ||||
chr10:71773490-71773607 | Common:2; Rare:41 | ||||
chr10:71819463-71819902 | Common:1; Rare:173; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71964158-71964566 | Common:5; Rare:113; Clinvar:1; Clinvar (benign):3 | ||||
chr10:72216215-72216514 | Common:2; Rare:90 | ||||
chr10:72273701-72273959 | Rare:78 |