Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:50723169-50723436 | Common:2; Rare:61 | ||||
chr19:51887894-51888052 | Rare:57 | ||||
chr19:52008180-52008349 | Rare:47 | ||||
chr19:52397725-52397889 | Common:5; Rare:51 | ||||
chr19:53333553-53333768 | Common:3; Rare:67 | ||||
chr19:53869438-53869736 | Common:2; Rare:79 | ||||
chr19:54102673-54102885 | Common:3; Rare:54 | ||||
chr19:54115289-54115473 | Common:2; Rare:50; Clinvar (benign):2 | ||||
chr19:54115635-54115797 | Common:1; Rare:37; Clinvar:4 | ||||
chr19:54200756-54200893 | Common:3; Rare:55 | ||||
chr19:54449039-54449264 | Common:2; Rare:68 | ||||
chr19:55258482-55258710 | Common:3; Rare:86 | ||||
chr19:55654897-55655067 | Rare:61 | ||||
chr19:56121511-56121599 | Common:1; Rare:22 | ||||
chr19:56368274-56368364 | Common:1; Rare:31 |