Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:12068834-12069018 | Common:1; Rare:76 | ||||
chr10:12129458-12129719 | Rare:107 | ||||
chr10:12195825-12196244 | Rare:115 | ||||
chr10:12349754-12349862 | Rare:35 | ||||
chr10:13099695-13099921 | Rare:53 | ||||
chr10:13099943-13100205 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):4 | ||||
chr10:13300044-13300164 | Rare:46; Clinvar:1 | ||||
chr10:13348009-13348319 | Rare:99 | ||||
chr10:14837984-14838389 | Common:2; Rare:120 | ||||
chr10:14878631-14878894 | Common:2; Rare:79 | ||||
chr10:14954023-14954194 | Rare:61 | ||||
chr10:15097306-15097401 | Common:1; Rare:46 | ||||
chr10:15860455-15860583 | Rare:36 | ||||
chr10:16817361-16817734 | Common:4; Rare:132 | ||||
chr10:17228788-17229026 | Common:3; Rare:60 |