Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:32971897-32972280 | Common:4; Rare:112 | ||||
chr19:33373554-33373878 | Common:2; Rare:104 | ||||
chr19:33521765-33521956 | Common:1; Rare:57; Clinvar:3 | ||||
chr19:34428312-34428453 | Rare:58 | ||||
chr19:34677239-34677348 | Common:1; Rare:25 | ||||
chr19:34677548-34677758 | Common:5; Rare:59 | ||||
chr19:34734135-34734291 | Common:1; Rare:48 | ||||
chr19:34926831-34926913 | Common:1; Rare:35 | ||||
chr19:35030856-35031283 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
chr19:35040310-35040545 | Common:1; Rare:47 | ||||
chr19:35138508-35138894 | Rare:85 | ||||
chr19:35138978-35139176 | Common:2; Rare:37 | ||||
chr19:35139290-35139509 | Common:3; Rare:38 | ||||
chr19:35139515-35140140 | Common:5; Rare:155 | ||||
chr19:35248942-35249016 | Common:1; Rare:39 |