Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:39920892-39921039 | Common:2; Rare:53 | ||||
chr15:40039094-40039311 | Rare:90 | ||||
chr15:40695076-40695218 | Rare:42 | ||||
chr15:40807424-40807761 | Common:4; Rare:113 | ||||
chr15:42273387-42273548 | Common:1; Rare:63 | ||||
chr15:42548740-42548932 | Common:1; Rare:102 | ||||
chr15:43330539-43330712 | Rare:65 | ||||
chr15:43371030-43371117 | Rare:20 | ||||
chr15:43746180-43746461 | Common:2; Rare:101 | ||||
chr15:43826924-43827022 | Rare:41 | ||||
chr15:44536897-44537193 | Common:1; Rare:104 | ||||
chr15:48645663-48645953 | Common:2; Rare:89; Clinvar (benign):1 | ||||
chr15:48878038-48878179 | Rare:53 | ||||
chr15:49155574-49155816 | Common:2; Rare:82 | ||||
chr15:49620794-49621091 | Common:6; Rare:121 |