Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:649233-649381 | Common:1; Rare:57 | ||||
chr16:670334-670503 | Rare:86 | ||||
chr16:680318-680499 | Common:2; Rare:60 | ||||
chr16:684326-684464 | Common:2; Rare:72 | ||||
chr16:1211003-1211216 | Common:5; Rare:99; Clinvar:2; Clinvar (benign):2 | ||||
chr16:1211305-1211606 | Common:2; Rare:146; Clinvar:3; Clinvar (benign):4 | ||||
chr16:1255878-1256085 | Common:2; Rare:46 | ||||
chr16:1351795-1351980 | Common:2; Rare:88; Clinvar:6; Clinvar (benign):1 | ||||
chr16:1420701-1420975 | Common:1; Rare:116 | ||||
chr16:1493233-1493357 | Common:1; Rare:48 | ||||
chr16:1533487-1533772 | Common:1; Rare:57 | ||||
chr16:1612042-1612342 | Common:1; Rare:97; Clinvar:1 | ||||
chr16:1706055-1706291 | Common:1; Rare:70 | ||||
chr16:1771488-1771613 | Rare:57 | ||||
chr16:1773117-1773319 | Rare:80 |