| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:55509704-55509983 | Common:3; Rare:50 | ||||
| chr16:55563739-55564036 | Common:1; Rare:38 | ||||
| chr16:55567424-55567687 | Common:1; Rare:64 | ||||
| chr16:56484718-56485044 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:57281548-57281722 | Common:2; Rare:35 | ||||
| chr16:57461230-57461351 | Rare:16; Clinvar:2 | ||||
| chr16:57790617-57790821 | Rare:25 | ||||
| chr16:57790849-57791005 | Common:2; Rare:23 | ||||
| chr16:57910700-57910858 | Common:3; Rare:20 | ||||
| chr16:57920662-57920892 | Rare:32 | ||||
| chr16:58016854-58017038 | Common:2; Rare:32 | ||||
| chr16:58541612-58541664 | Rare:10 | ||||
| chr16:58587214-58587395 | Rare:43 | ||||
| chr16:61055435-61055693 | Common:1; Rare:55 | ||||
| chr16:66617540-66617712 | Rare:29 |