| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:684326-684475 | Common:3; Rare:81 | ||||
| chr16:690389-690436 | Common:1; Rare:21 | ||||
| chr16:721053-721172 | Common:2; Rare:28 | ||||
| chr16:740968-741145 | Rare:57 | ||||
| chr16:970851-971194 | Common:7; Rare:156 | ||||
| chr16:1225754-1225965 | Common:5; Rare:77 | ||||
| chr16:1309391-1309721 | Rare:123 | ||||
| chr16:1315560-1315706 | Rare:44 | ||||
| chr16:1333536-1333652 | Common:1; Rare:53 | ||||
| chr16:1420705-1420957 | Common:1; Rare:105 | ||||
| chr16:1493229-1493414 | Common:3; Rare:65 | ||||
| chr16:1533460-1533688 | Common:2; Rare:48 | ||||
| chr16:1612042-1612385 | Common:2; Rare:122; Clinvar:1 | ||||
| chr16:1706047-1706651 | Common:5; Rare:163; Clinvar (pathogenic):1 | ||||
| chr16:1768322-1768533 | Common:1; Rare:78 |