Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:37412295-37412448 | Rare:34 | ||||
chr20:37412900-37412935 | Rare:8 | ||||
chr20:37422073-37422207 | Common:2; Rare:32 | ||||
chr20:38446574-38446716 | Common:1; Rare:44 | ||||
chr20:44738942-44739056 | Common:1; Rare:28 | ||||
chr20:44886383-44886445 | Rare:14 | ||||
chr20:45293166-45293215 | Rare:10 | ||||
chr20:45424261-45424576 | Common:3; Rare:89; Clinvar (pathogenic):1 | ||||
chr20:47357794-47357890 | Rare:15 | ||||
chr20:64092178-64092271 | Common:1; Rare:22 | ||||
chr21:16070432-16070557 | Rare:25 | ||||
chr21:16071064-16071226 | Rare:50 | ||||
chr21:16071232-16071322 | Rare:35 | ||||
chr21:16073625-16073719 | Common:1; Rare:26 | ||||
chr21:16073722-16074037 | Common:1; Rare:48 |