Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:46298120-46298443 | Common:5; Rare:77 | ||||
chr19:46346941-46347143 | Common:3; Rare:69 | ||||
chr19:46413438-46413767 | Common:1; Rare:94 | ||||
chr19:46471480-46471523 | Common:3; Rare:25 | ||||
chr19:46600913-46601094 | Common:2; Rare:74 | ||||
chr19:46601200-46601409 | Common:3; Rare:63; Clinvar (benign):1 | ||||
chr19:46717080-46717264 | Common:2; Rare:64 | ||||
chr19:46745835-46746066 | Common:3; Rare:46 | ||||
chr19:46787283-46787382 | Rare:20 | ||||
chr19:47112152-47112505 | Rare:115 | ||||
chr19:47256460-47256577 | Rare:45 | ||||
chr19:47484201-47484300 | Common:1; Rare:30 | ||||
chr19:48170243-48170699 | Common:2; Rare:127 | ||||
chr19:48321306-48321506 | Common:1; Rare:67 | ||||
chr19:48325314-48325609 | Common:2; Rare:63 |