Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:47717154-47717540 | Common:1; Rare:83 | ||||
chr15:47717909-47718103 | Common:2; Rare:45 | ||||
chr15:48178128-48178431 | Common:1; Rare:93 | ||||
chr15:48331367-48331465 | Rare:32 | ||||
chr15:48645710-48645816 | Common:1; Rare:31; Clinvar (benign):1 | ||||
chr15:48877998-48878635 | Common:1; Rare:237 | ||||
chr15:48963917-48964030 | Rare:14 | ||||
chr15:49046354-49046549 | Rare:81 | ||||
chr15:49155546-49155859 | Common:2; Rare:102 | ||||
chr15:49170128-49170283 | Rare:32 | ||||
chr15:49620794-49621121 | Common:6; Rare:130 | ||||
chr15:50354931-50354998 | Rare:10 | ||||
chr15:50355068-50355513 | Common:3; Rare:179 | ||||
chr15:50424112-50424466 | Common:2; Rare:129 | ||||
chr15:50686679-50686937 | Common:5; Rare:103 |