Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2716543-2716729 | Common:1; Rare:36 | ||||
chr16:4891067-4891369 | Common:3; Rare:75 | ||||
chr16:4894724-4895003 | Rare:57 | ||||
chr16:4896231-4896304 | Rare:17 | ||||
chr16:4896318-4896529 | Rare:43 | ||||
chr16:4897675-4897861 | Common:1; Rare:63 | ||||
chr16:4919181-4919330 | Common:2; Rare:39 | ||||
chr16:4934046-4934370 | Common:3; Rare:85 | ||||
chr16:8815350-8815626 | Common:3; Rare:70 | ||||
chr16:15008684-15008787 | Rare:25 | ||||
chr16:15704013-15704355 | Common:2; Rare:103; Clinvar:6; Clinvar (benign):5 | ||||
chr16:15720149-15720421 | Common:1; Rare:92; Clinvar:12; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
chr16:15747568-15747866 | Rare:72; Clinvar:7; Clinvar (benign):2 | ||||
chr16:21820398-21820524 | Rare:34 | ||||
chr16:29139595-29139699 | Common:2; Rare:20 |