Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68901049-68901389 | Common:3; Rare:133 | ||||
chr10:69087992-69088209 | Rare:44 | ||||
chr10:69179943-69180302 | Common:2; Rare:114 | ||||
chr10:71819556-71819801 | Common:1; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
chr10:72273588-72273937 | Rare:88 | ||||
chr10:72354881-72355054 | Common:2; Rare:81 | ||||
chr10:73167941-73168292 | Rare:96 | ||||
chr10:73252589-73252802 | Rare:58; Clinvar:4 | ||||
chr10:73495606-73495764 | Rare:31 | ||||
chr10:73495818-73496140 | Common:2; Rare:91 | ||||
chr10:73744002-73744090 | Rare:27 | ||||
chr10:73744248-73744436 | Common:1; Rare:51 | ||||
chr10:73772420-73772712 | Rare:136 | ||||
chr10:73781951-73782084 | Common:1; Rare:43 | ||||
chr10:73874500-73874738 | Rare:58 |