Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68900964-68901377 | Common:3; Rare:160 | ||||
chr10:68956061-68956234 | Rare:66 | ||||
chr10:69087902-69088144 | Rare:55 | ||||
chr10:70163529-70163802 | Common:4; Rare:53 | ||||
chr10:71773494-71773730 | Common:3; Rare:69 | ||||
chr10:71819465-71819899 | Common:1; Rare:172; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851185-71851467 | Common:5; Rare:116; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216237-72216487 | Common:1; Rare:78 | ||||
chr10:72273700-72274103 | Rare:119 | ||||
chr10:72354895-72355058 | Common:2; Rare:81 | ||||
chr10:73096790-73097033 | Common:3; Rare:74 | ||||
chr10:73167939-73168138 | Rare:51 | ||||
chr10:73252617-73252759 | Rare:41; Clinvar:2 | ||||
chr10:73495593-73495763 | Rare:35 | ||||
chr10:73495806-73496114 | Common:2; Rare:86 |