| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56729857-56730257 | Common:7; Rare:453 | ||||
| chr16:56931866-56932324 | Common:14; Rare:874 | ||||
| chr16:56932460-56932702 | Common:3; Rare:63 | ||||
| chr16:56932760-56934026 | Common:12; Rare:346 | ||||
| chr16:57091990-57092330 | Common:2; Rare:59 | ||||
| chr16:57092360-57092760 | Common:16; Rare:223 | ||||
| chr16:57145144-57145544 | Common:1; Rare:53 | ||||
| chr16:57145721-57146121 | Common:2; Rare:107 | ||||
| chr16:57185162-57185680 | Rare:263 | ||||
| chr16:57185807-57186407 | Common:9; Rare:902 | ||||
| chr16:57244750-57245392 | Common:23; Rare:857 | ||||
| chr16:57245669-57245783 | Rare:32 | ||||
| chr16:57284495-57285051 | Common:17; Rare:439 | ||||
| chr16:57446528-57447706 | Common:23; Rare:585; Clinvar:12; Clinvar (benign):16 | ||||
| chr16:57462340-57462751 | Common:4; Rare:271 |