| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56519910-56520161 | Common:8; Rare:154; Clinvar:12; Clinvar (benign):10 | ||||
| chr16:56608362-56608760 | Common:6; Rare:215 | ||||
| chr16:56625589-56625804 | Common:1; Rare:94 | ||||
| chr16:56682229-56682486 | Common:8; Rare:122 | ||||
| chr16:56729941-56730212 | Common:2; Rare:130 | ||||
| chr16:56865069-56865317 | Common:2; Rare:121; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr16:56931885-56932267 | Common:6; Rare:359 | ||||
| chr16:56932690-56933280 | Common:7; Rare:144 | ||||
| chr16:56989360-56989618 | Common:2; Rare:111; Clinvar:2 | ||||
| chr16:57092446-57092635 | Common:6; Rare:70 | ||||
| chr16:57185754-57186429 | Common:6; Rare:338 | ||||
| chr16:57244945-57245374 | Common:6; Rare:278 | ||||
| chr16:57284567-57284793 | Common:6; Rare:136 | ||||
| chr16:57447336-57447544 | Common:4; Rare:123; Clinvar:4; Clinvar (benign):6 | ||||
| chr16:57535890-57536320 | Common:4; Rare:290 |