Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:52923414-52923559 | Common:2; Rare:59 | ||||
chr19:52942563-52942736 | Common:6; Rare:61 | ||||
chr19:55546109-55546318 | Common:1; Rare:44 | ||||
chr2:3473096-3473233 | Common:3; Rare:32 | ||||
chr2:8733398-8733470 | Rare:17 | ||||
chr2:9484182-9484483 | Common:1; Rare:66 | ||||
chr2:12716016-12716095 | Common:1; Rare:14 | ||||
chr2:13000806-13000952 | Common:1; Rare:37 | ||||
chr2:19347990-19348113 | Common:1; Rare:47 | ||||
chr2:20447729-20447850 | Rare:33 | ||||
chr2:20447860-20447906 | Rare:8 | ||||
chr2:20448678-20448820 | Common:1; Rare:31 | ||||
chr2:21042400-21042539 | Rare:44; Clinvar:4; Clinvar (benign):2 | ||||
chr2:25822104-25822349 | Common:6; Rare:55 | ||||
chr2:27265169-27265293 | Rare:27 |