| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:53098996-53099189 | Rare:41 | ||||
| chr16:53703815-53704199 | Rare:118; Clinvar:4; Clinvar (benign):1 | ||||
| chr16:54286722-54287011 | Common:1; Rare:87 | ||||
| chr16:56451303-56451605 | Common:1; Rare:99 | ||||
| chr16:56608408-56608776 | Common:3; Rare:109 | ||||
| chr16:56682118-56682513 | Common:8; Rare:111 | ||||
| chr16:56729949-56730205 | Common:1; Rare:62 | ||||
| chr16:56931902-56932178 | Common:3; Rare:139 | ||||
| chr16:56989482-56989598 | Common:1; Rare:25 | ||||
| chr16:57185784-57186371 | Common:3; Rare:165 | ||||
| chr16:57245155-57245262 | Rare:31 | ||||
| chr16:57447347-57447527 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:57628391-57628709 | Common:3; Rare:75 | ||||
| chr16:57764333-57764490 | Rare:33 | ||||
| chr16:58001336-58001646 | Common:1; Rare:115; Clinvar (benign):1 |