Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:3977213-3977633 | Common:4; Rare:140; Clinvar (benign):8 | ||||
chr19:4035802-4035964 | Common:14; Rare:19 | ||||
chr19:4043178-4043357 | Common:1; Rare:54 | ||||
chr19:4456391-4456436 | Rare:7 | ||||
chr19:4456595-4456777 | Rare:40 | ||||
chr19:4792745-4793049 | Rare:86 | ||||
chr19:4944265-4944369 | Rare:43 | ||||
chr19:5205568-5205676 | Common:2; Rare:32 | ||||
chr19:5209609-5209966 | Common:2; Rare:73 | ||||
chr19:5240139-5240228 | Common:1; Rare:38 | ||||
chr19:5247490-5247548 | Common:1; Rare:7 | ||||
chr19:5247748-5248083 | Common:3; Rare:79 | ||||
chr19:5256295-5256364 | Rare:7 | ||||
chr19:5894415-5894701 | Common:2; Rare:91; Clinvar:3 | ||||
chr19:6184684-6184832 | Rare:21 |