Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69801609-69802073 | Common:3; Rare:105 | ||||
chr10:70052742-70052935 | Rare:41 | ||||
chr10:70132815-70132906 | Rare:18 | ||||
chr10:70146638-70146983 | Common:2; Rare:80 | ||||
chr10:70170448-70170722 | Common:3; Rare:86 | ||||
chr10:70233348-70233566 | Common:5; Rare:77 | ||||
chr10:70382570-70382881 | Common:5; Rare:117 | ||||
chr10:70403971-70404176 | Rare:78 | ||||
chr10:70815830-70816081 | Rare:90 | ||||
chr10:70887867-70887940 | Common:1; Rare:14 | ||||
chr10:70888520-70888649 | Common:1; Rare:46; Clinvar:5; Clinvar (benign):1 | ||||
chr10:71819601-71819805 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr10:71851204-71851452 | Common:5; Rare:107; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:71964436-71964565 | Common:4; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
chr10:72273701-72273988 | Rare:90 |