Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44643801-44643918 | Rare:35 | ||||
chr19:45370548-45370731 | Common:2; Rare:53 | ||||
chr19:45405038-45405246 | Common:1; Rare:45 | ||||
chr19:45406355-45406687 | Common:2; Rare:83 | ||||
chr19:45423509-45423659 | Common:2; Rare:31; Clinvar (benign):1 | ||||
chr19:45423872-45423992 | Common:2; Rare:23 | ||||
chr19:45507228-45507516 | Common:1; Rare:74 | ||||
chr19:45692365-45692713 | Common:1; Rare:81 | ||||
chr19:46600965-46601402 | Common:5; Rare:144 | ||||
chr19:47256460-47256583 | Rare:48 | ||||
chr19:48170259-48170696 | Common:2; Rare:119 | ||||
chr19:48445886-48446020 | Rare:48 | ||||
chr19:48619139-48619320 | Rare:68 | ||||
chr19:48811003-48811126 | Rare:43 | ||||
chr19:48900197-48900367 | Common:1; Rare:60 |