Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:50990727-50990933 | Common:3; Rare:35 | ||||
chr10:51074029-51074328 | Common:5; Rare:74 | ||||
chr10:51074391-51074808 | Common:1; Rare:106; Clinvar (benign):11 | ||||
chr10:51699547-51699676 | Common:1; Rare:48 | ||||
chr10:56361232-56361473 | Common:5; Rare:75 | ||||
chr10:58268937-58269290 | Common:6; Rare:116 | ||||
chr10:58334881-58335076 | Rare:61 | ||||
chr10:58385313-58385577 | Common:2; Rare:93 | ||||
chr10:59362469-59362703 | Common:1; Rare:67 | ||||
chr10:59709570-59709914 | Common:2; Rare:85 | ||||
chr10:59906836-59907037 | Rare:46 | ||||
chr10:60140688-60140852 | Common:1; Rare:31 | ||||
chr10:60300499-60300567 | Rare:17 | ||||
chr10:60572624-60572708 | Rare:19 | ||||
chr10:60572852-60572970 | Rare:17 |