Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35637672-35637811 | Common:1; Rare:19 | ||||
chr19:36125425-36125781 | Rare:117 | ||||
chr19:36142180-36142332 | Common:1; Rare:54 | ||||
chr19:36142511-36142756 | Common:1; Rare:73 | ||||
chr19:36142904-36143138 | Rare:56 | ||||
chr19:36145949-36146339 | Common:1; Rare:119 | ||||
chr19:36797491-36797541 | Rare:14 | ||||
chr19:37946285-37946582 | Common:2; Rare:57 | ||||
chr19:38135815-38136011 | Common:1; Rare:43 | ||||
chr19:38267331-38267448 | Common:1; Rare:15 | ||||
chr19:38267766-38267921 | Common:1; Rare:33 | ||||
chr19:38657800-38658092 | Common:1; Rare:51 | ||||
chr19:38684124-38684285 | Common:2; Rare:27 | ||||
chr19:38700601-38701118 | Common:4; Rare:130; Clinvar (benign):2 | ||||
chr19:39197836-39197973 | Rare:18 |