Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68331914-68332129 | Common:1; Rare:93 | ||||
chr10:68332884-68333032 | Common:1; Rare:36 | ||||
chr10:68407187-68407362 | Common:4; Rare:59 | ||||
chr10:68720927-68721282 | Common:2; Rare:115 | ||||
chr10:68901054-68901361 | Common:3; Rare:120 | ||||
chr10:68956093-68956423 | Common:3; Rare:107 | ||||
chr10:68988749-68988826 | Common:1; Rare:29; Clinvar (benign):2 | ||||
chr10:69087927-69088158 | Rare:49 | ||||
chr10:69179943-69180301 | Common:2; Rare:112 | ||||
chr10:70170414-70170670 | Common:4; Rare:87 | ||||
chr10:71773504-71773711 | Common:3; Rare:59 | ||||
chr10:71819533-71819897 | Common:1; Rare:150; Clinvar:4; Clinvar (benign):4 | ||||
chr10:71821982-71822047 | Rare:16; Clinvar:1 | ||||
chr10:71851181-71851464 | Common:5; Rare:120; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216232-72216530 | Common:3; Rare:90 |