Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37469262-37469392 | Common:2; Rare:37 | ||||
chr19:37594728-37594910 | Rare:50 | ||||
chr19:37779579-37779670 | Rare:18 | ||||
chr19:38264804-38264997 | Rare:60 | ||||
chr19:38724003-38724461 | Rare:168; Clinvar:1; Clinvar (benign):2 | ||||
chr19:38789097-38789216 | Common:2; Rare:14 | ||||
chr19:38790535-38790735 | Rare:31 | ||||
chr19:38852319-38852402 | Rare:19 | ||||
chr19:38899572-38900020 | Rare:132 | ||||
chr19:38930732-38930988 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39084044-39084399 | Common:2; Rare:92 | ||||
chr19:39156422-39156697 | Common:2; Rare:57 | ||||
chr19:39197115-39197253 | Rare:50 | ||||
chr19:39390850-39391436 | Common:1; Rare:222 | ||||
chr19:39406684-39406925 | Rare:92 |