Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:71484499-71484773 | Common:2; Rare:53 | ||||
chr16:71564824-71565118 | Common:2; Rare:92 | ||||
chr16:71565205-71565277 | Rare:17 | ||||
chr16:71723099-71723330 | Common:2; Rare:60 | ||||
chr16:71723554-71723662 | Rare:28 | ||||
chr16:71723775-71724100 | Common:5; Rare:111 | ||||
chr16:71808506-71808895 | Common:1; Rare:176 | ||||
chr16:71809025-71809394 | Common:3; Rare:122 | ||||
chr16:71845793-71846047 | Common:2; Rare:82 | ||||
chr16:71883281-71883615 | Rare:85 | ||||
chr16:71884082-71884422 | Common:1; Rare:115 | ||||
chr16:71894327-71894480 | Rare:41 | ||||
chr16:71894517-71894770 | Rare:45 | ||||
chr16:71894965-71895648 | Common:4; Rare:250 | ||||
chr16:72008462-72008885 | Common:6; Rare:172; Clinvar (benign):2 |