Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:61662825-61662983 | Rare:43 | ||||
chr10:62049188-62049477 | Common:2; Rare:67 | ||||
chr10:68074669-68074937 | Common:1; Rare:66 | ||||
chr10:68332861-68333294 | Common:2; Rare:97 | ||||
chr10:68755811-68756072 | Common:2; Rare:35 | ||||
chr10:68787967-68788199 | Common:1; Rare:58 | ||||
chr10:68988580-68988847 | Common:1; Rare:70; Clinvar (benign):2 | ||||
chr10:69087966-69088144 | Rare:41 | ||||
chr10:69801615-69801987 | Common:2; Rare:94 | ||||
chr10:70170416-70170749 | Common:4; Rare:106 | ||||
chr10:71819465-71819892 | Common:1; Rare:170; Clinvar:5; Clinvar (benign):3 | ||||
chr10:72216237-72216544 | Common:3; Rare:89 | ||||
chr10:73096742-73097032 | Common:4; Rare:86 | ||||
chr10:73167970-73168172 | Rare:53 | ||||
chr10:73252556-73252773 | Common:2; Rare:64; Clinvar:5; Clinvar (benign):2 |