Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:34224978-34225135 | Rare:62 | ||||
chr15:34343042-34343419 | Common:4; Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
chr15:34437406-34437688 | Common:1; Rare:60 | ||||
chr15:34582808-34582895 | Rare:26 | ||||
chr15:34588447-34588569 | Rare:35 | ||||
chr15:34988197-34988409 | Common:1; Rare:88 | ||||
chr15:35546128-35546263 | Common:1; Rare:49 | ||||
chr15:37100372-37100801 | Common:1; Rare:136 | ||||
chr15:37101280-37101383 | Common:23; Rare:49 | ||||
chr15:38454044-38454200 | Rare:58 | ||||
chr15:39782794-39782893 | Rare:26 | ||||
chr15:39920930-39921060 | Common:2; Rare:47 | ||||
chr15:40039092-40039349 | Rare:101 | ||||
chr15:40358074-40358324 | Common:8; Rare:105 | ||||
chr15:40405643-40405830 | Common:2; Rare:57; Clinvar (benign):3; Clinvar (pathogenic):3 |