Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68331899-68332180 | Common:2; Rare:113 | ||||
chr10:68332697-68332715 | Rare:8 | ||||
chr10:68332877-68333008 | Common:1; Rare:35 | ||||
chr10:68407185-68407413 | Common:4; Rare:78 | ||||
chr10:68471887-68472033 | Common:1; Rare:77; Clinvar (benign):1 | ||||
chr10:68721090-68721282 | Common:2; Rare:62 | ||||
chr10:68956093-68956415 | Common:3; Rare:106 | ||||
chr10:68988598-68988913 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):4 | ||||
chr10:68989020-68989105 | Common:1; Rare:26; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:69087974-69088203 | Rare:49 | ||||
chr10:70052758-70052978 | Rare:49 | ||||
chr10:70233348-70233564 | Common:5; Rare:75 | ||||
chr10:70382583-70382803 | Common:5; Rare:83 | ||||
chr10:70815815-70816002 | Rare:71 | ||||
chr10:70887867-70888016 | Common:1; Rare:28 |