| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2083451-2083683 | Common:1; Rare:94; Clinvar:4; Clinvar (benign):2 | ||||
| chr16:2107159-2107306 | Common:4; Rare:57 | ||||
| chr16:2223375-2223766 | Rare:149 | ||||
| chr16:2264467-2264575 | Rare:27 | ||||
| chr16:2267775-2268220 | Common:3; Rare:186 | ||||
| chr16:2268374-2268506 | Common:1; Rare:47 | ||||
| chr16:2429148-2429481 | Common:2; Rare:110 | ||||
| chr16:2459957-2460161 | Common:2; Rare:58 | ||||
| chr16:2474949-2475165 | Rare:67; Clinvar (benign):2 | ||||
| chr16:2482894-2483046 | Common:2; Rare:25 | ||||
| chr16:2514009-2514172 | Common:1; Rare:75 | ||||
| chr16:2519037-2519401 | Rare:89 | ||||
| chr16:2520056-2520456 | Common:9; Rare:205 | ||||
| chr16:2537677-2538119 | Common:4; Rare:169 | ||||
| chr16:2682349-2682717 | Rare:166 |