| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56951510-56951850 | Common:4; Rare:60 | ||||
| chr16:56970404-56970804 | Common:4; Rare:124 | ||||
| chr16:56971010-56971720 | Common:14; Rare:347; Clinvar:3; Clinvar (benign):4 | ||||
| chr16:56972897-56973513 | Common:6; Rare:209; Clinvar (benign):2 | ||||
| chr16:56980630-56981240 | Common:9; Rare:131; Clinvar (benign):3 | ||||
| chr16:56981410-56981810 | Common:12; Rare:144; Clinvar (benign):2 | ||||
| chr16:56982995-56983191 | Common:3; Rare:29 | ||||
| chr16:56985020-56985235 | Common:2; Rare:36 | ||||
| chr16:56985181-56985969 | Common:6; Rare:323 | ||||
| chr16:56988774-56988959 | Common:1; Rare:30; Clinvar:1 | ||||
| chr16:56990324-56990552 | Common:1; Rare:34 | ||||
| chr16:56990756-56990877 | Rare:15 | ||||
| chr16:56990891-56991363 | Common:7; Rare:140 | ||||
| chr16:56991733-56992133 | Common:3; Rare:150 | ||||
| chr16:56999139-56999908 | Common:4; Rare:252 |