Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36528224-36528280 | Common:1; Rare:18 | ||||
chr19:36573252-36573448 | Common:3; Rare:58 | ||||
chr19:36605254-36605310 | Rare:15 | ||||
chr19:36687388-36687631 | Common:3; Rare:78 | ||||
chr19:36772795-36773116 | Common:4; Rare:81 | ||||
chr19:37210513-37210594 | Common:1; Rare:19 | ||||
chr19:37467177-37467519 | Common:2; Rare:99 | ||||
chr19:38618923-38619271 | Common:3; Rare:103 | ||||
chr19:38899615-38900023 | Rare:115 | ||||
chr19:38930738-38931002 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39390991-39391419 | Common:1; Rare:163 | ||||
chr19:39406710-39406848 | Rare:52 | ||||
chr19:39435906-39436154 | Common:4; Rare:87 | ||||
chr19:39480752-39480925 | Common:3; Rare:93; Clinvar (pathogenic):1 | ||||
chr19:39846326-39846473 | Common:1; Rare:67 |