| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56971237-56971538 | Common:3; Rare:75; Clinvar (benign):1 | ||||
| chr16:56980820-56981012 | Common:2; Rare:37 | ||||
| chr16:56988248-56988550 | Common:1; Rare:49 | ||||
| chr16:56990246-56990581 | Common:1; Rare:48 | ||||
| chr16:56990925-56991052 | Common:1; Rare:22 | ||||
| chr16:56991811-56992024 | Common:1; Rare:49 | ||||
| chr16:57000108-57000184 | Common:1; Rare:16 | ||||
| chr16:57000670-57000935 | Common:5; Rare:42 | ||||
| chr16:57005049-57005093 | Rare:7 | ||||
| chr16:57014696-57014731 | Rare:10 | ||||
| chr16:57042042-57042067 | Rare:6 | ||||
| chr16:57042211-57042477 | Rare:47 | ||||
| chr16:57260356-57260398 | Rare:8 | ||||
| chr16:57299517-57299657 | Rare:28 | ||||
| chr16:57299875-57299949 | Common:5; Rare:38 |