| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87765914-87766044 | Rare:49 | ||||
| chr16:87836035-87836315 | Common:1; Rare:84 | ||||
| chr16:87837187-87837322 | Common:3; Rare:24 | ||||
| chr16:88570167-88570489 | Common:2; Rare:123 | ||||
| chr16:88663070-88663362 | Common:7; Rare:119 | ||||
| chr16:88706194-88706542 | Common:4; Rare:153 | ||||
| chr16:88856870-88857183 | Common:4; Rare:151; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89217612-89217765 | Common:1; Rare:77 | ||||
| chr16:89508296-89508428 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:89560541-89560739 | Rare:89 | ||||
| chr16:89657631-89658095 | Common:3; Rare:243 | ||||
| chr16:89686574-89686706 | Common:6; Rare:61 | ||||
| chr16:89686898-89686957 | Rare:24 | ||||
| chr16:89711676-89711896 | Common:3; Rare:86 | ||||
| chr16:89720865-89721049 | Common:1; Rare:59 |