Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49665777-49666020 | Common:2; Rare:124; Clinvar (pathogenic):1 | ||||
chr19:49877319-49877531 | Rare:46 | ||||
chr19:49877641-49877726 | Rare:34 | ||||
chr19:49929430-49929838 | Common:7; Rare:138 | ||||
chr19:50476232-50476544 | Common:1; Rare:145 | ||||
chr19:50511169-50511401 | Common:1; Rare:75 | ||||
chr19:50723179-50723377 | Common:2; Rare:49 | ||||
chr19:50804582-50804909 | Common:6; Rare:101 | ||||
chr19:51751866-51751978 | Common:2; Rare:23 | ||||
chr19:52008143-52008349 | Rare:61 | ||||
chr19:52028360-52028465 | Common:2; Rare:19 | ||||
chr19:52171443-52171733 | Common:3; Rare:71 | ||||
chr19:52269427-52269603 | Common:1; Rare:61 | ||||
chr19:52397711-52397885 | Common:3; Rare:52 | ||||
chr19:52897612-52897917 | Rare:85 |