Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68560267-68560426 | Rare:33 | ||||
chr10:68721125-68721282 | Common:1; Rare:55 | ||||
chr10:68721422-68721534 | Common:2; Rare:35 | ||||
chr10:68901040-68901368 | Common:3; Rare:127 | ||||
chr10:68956093-68956423 | Common:3; Rare:107 | ||||
chr10:68988540-68988847 | Common:1; Rare:75; Clinvar (benign):2 | ||||
chr10:69087980-69088236 | Rare:55 | ||||
chr10:69179918-69180341 | Common:3; Rare:140 | ||||
chr10:69318686-69318967 | Common:4; Rare:84 | ||||
chr10:69451314-69451592 | Common:2; Rare:79 | ||||
chr10:70132721-70132906 | Rare:51 | ||||
chr10:70146657-70146844 | Common:1; Rare:46 | ||||
chr10:70170425-70170682 | Common:4; Rare:86 | ||||
chr10:70233296-70233557 | Common:6; Rare:97; Clinvar (benign):1 | ||||
chr10:70403914-70404191 | Common:1; Rare:105 |