Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69087972-69088209 | Rare:50 | ||||
chr10:69801778-69801910 | Common:1; Rare:35 | ||||
chr10:70132807-70132882 | Rare:17 | ||||
chr10:70170454-70170719 | Common:3; Rare:85 | ||||
chr10:70233319-70233566 | Common:6; Rare:89; Clinvar (benign):1 | ||||
chr10:70403983-70404158 | Rare:65 | ||||
chr10:70815830-70815999 | Rare:66 | ||||
chr10:71819549-71819897 | Common:1; Rare:145; Clinvar:3; Clinvar (benign):4 | ||||
chr10:71851204-71851452 | Common:5; Rare:107; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72273709-72273981 | Rare:86 | ||||
chr10:72354869-72355163 | Common:2; Rare:106 | ||||
chr10:73096746-73097028 | Common:4; Rare:85 | ||||
chr10:73167958-73168142 | Rare:44 | ||||
chr10:73252563-73252791 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):2 | ||||
chr10:73495590-73495771 | Rare:39 |