Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1174218-1174384 | Common:1; Rare:77 | ||||
chr19:1248432-1248604 | Common:1; Rare:58 | ||||
chr19:1269047-1269407 | Common:2; Rare:139 | ||||
chr19:1354833-1355008 | Rare:71 | ||||
chr19:1401484-1401621 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):4 | ||||
chr19:1479168-1479345 | Common:1; Rare:65 | ||||
chr19:1490309-1490474 | Common:3; Rare:58 | ||||
chr19:1605369-1605592 | Common:3; Rare:87 | ||||
chr19:1905170-1905434 | Common:4; Rare:111 | ||||
chr19:1942444-1942609 | Rare:42 | ||||
chr19:2096090-2096407 | Rare:102 | ||||
chr19:2269238-2269601 | Common:2; Rare:153 | ||||
chr19:2269664-2269865 | Common:4; Rare:90 | ||||
chr19:2328559-2328721 | Common:2; Rare:79 | ||||
chr19:2475868-2476242 | Common:2; Rare:129 |