Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:61453315-61453541 | Common:1; Rare:42 | ||||
chr10:62816360-62816529 | Rare:29 | ||||
chr10:68075189-68075509 | Common:4; Rare:133 | ||||
chr10:68331886-68332134 | Common:2; Rare:104 | ||||
chr10:68332890-68333039 | Common:1; Rare:38 | ||||
chr10:68407252-68407415 | Common:3; Rare:51 | ||||
chr10:69087967-69088218 | Rare:55 | ||||
chr10:71773472-71773704 | Common:3; Rare:73 | ||||
chr10:71851217-71851330 | Common:3; Rare:59; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr10:72273704-72273942 | Rare:64 | ||||
chr10:72354881-72355023 | Common:2; Rare:69 | ||||
chr10:73096770-73097033 | Common:3; Rare:79 | ||||
chr10:73167970-73168141 | Rare:41 | ||||
chr10:73252594-73252765 | Rare:48; Clinvar:4 | ||||
chr10:73495575-73495753 | Rare:34 |