| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56657629-56658043 | Common:3; Rare:110 | ||||
| chr16:56682304-56682504 | Common:3; Rare:69 | ||||
| chr16:56729929-56730194 | Common:1; Rare:63 | ||||
| chr16:56781577-56782170 | Common:2; Rare:111 | ||||
| chr16:56783513-56783743 | Common:1; Rare:34 | ||||
| chr16:56931902-56932197 | Common:3; Rare:152 | ||||
| chr16:57185625-57185691 | Common:1; Rare:9 | ||||
| chr16:57185728-57186477 | Common:5; Rare:208 | ||||
| chr16:57244964-57245262 | Common:3; Rare:99 | ||||
| chr16:57372367-57372498 | Rare:27 | ||||
| chr16:57447321-57447556 | Common:4; Rare:77; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:57479554-57479938 | Common:2; Rare:80 | ||||
| chr16:57639294-57639557 | Common:1; Rare:57; Clinvar (pathogenic):1 | ||||
| chr16:57736616-57736716 | Rare:20 | ||||
| chr16:57999426-57999755 | Rare:61 |