Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:19192115-19192216 | Common:1; Rare:37 | ||||
chr19:19192624-19193009 | Common:3; Rare:89; Clinvar (benign):1 | ||||
chr19:19320485-19320850 | Common:4; Rare:129 | ||||
chr19:19516167-19516253 | Rare:41 | ||||
chr19:19628210-19628312 | Rare:24 | ||||
chr19:19668606-19668810 | Rare:48 | ||||
chr19:19821708-19821878 | Common:1; Rare:57 | ||||
chr19:19900807-19900993 | Common:1; Rare:48 | ||||
chr19:20661535-20661726 | Common:6; Rare:55 | ||||
chr19:22532460-22532702 | Common:2; Rare:63 | ||||
chr19:29213131-29213219 | Common:1; Rare:34 | ||||
chr19:29606172-29606320 | Rare:49 | ||||
chr19:29665253-29665461 | Common:4; Rare:76 | ||||
chr19:32405551-32405806 | Rare:110 | ||||
chr19:32406020-32406156 | Rare:41 |