Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39344589-39344668 | Rare:19 | ||||
chr19:39410505-39410760 | Common:1; Rare:55 | ||||
chr19:39459812-39459937 | Rare:35 | ||||
chr19:39473285-39473491 | Rare:49 | ||||
chr19:39474238-39474560 | Rare:84 | ||||
chr19:39539211-39539429 | Common:1; Rare:46 | ||||
chr19:40045577-40045851 | Common:3; Rare:38 | ||||
chr19:40356484-40356878 | Common:1; Rare:66 | ||||
chr19:40378470-40378530 | Rare:9 | ||||
chr19:40607247-40607560 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):2 | ||||
chr19:40620157-40620218 | Common:1; Rare:15 | ||||
chr19:40808415-40808562 | Rare:24 | ||||
chr19:41236771-41236903 | Common:1; Rare:21 | ||||
chr19:41238476-41238739 | Rare:65 | ||||
chr19:41238749-41238818 | Rare:12 |