Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70403947-70404196 | Rare:94 | ||||
chr10:70478130-70478830 | Common:2; Rare:197 | ||||
chr10:70672304-70672553 | Common:2; Rare:103 | ||||
chr10:70815788-70816053 | Rare:98 | ||||
chr10:70887852-70887994 | Common:1; Rare:29 | ||||
chr10:70888219-70888404 | Common:2; Rare:41 | ||||
chr10:70888526-70888653 | Common:1; Rare:43; Clinvar:5; Clinvar (benign):1 | ||||
chr10:71212359-71212572 | Common:1; Rare:65 | ||||
chr10:71319280-71319883 | Common:6; Rare:184; Clinvar:1 | ||||
chr10:71396649-71396965 | Common:3; Rare:73 | ||||
chr10:71851235-71851468 | Common:3; Rare:90; Clinvar:3; Clinvar (benign):6 | ||||
chr10:71964137-71964445 | Common:1; Rare:87 | ||||
chr10:72215915-72216095 | Rare:72 | ||||
chr10:72216252-72216403 | Rare:61 | ||||
chr10:72273602-72273945 | Rare:89 |