| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2223121-2223721 | Rare:206 | ||||
| chr16:2223984-2224249 | Rare:63 | ||||
| chr16:2233718-2233764 | Rare:8 | ||||
| chr16:2250919-2251239 | Common:1; Rare:79 | ||||
| chr16:2251316-2251437 | Rare:44 | ||||
| chr16:2251497-2251866 | Common:3; Rare:124 | ||||
| chr16:2267650-2267720 | Rare:28 | ||||
| chr16:2267823-2267947 | Rare:47 | ||||
| chr16:2267986-2268253 | Common:1; Rare:123 | ||||
| chr16:2268331-2268593 | Common:3; Rare:91 | ||||
| chr16:2339819-2340157 | Common:1; Rare:72 | ||||
| chr16:2340258-2340365 | Rare:29 | ||||
| chr16:2340629-2341087 | Common:4; Rare:153; Clinvar:3; Clinvar (benign):2 | ||||
| chr16:2429042-2429546 | Common:4; Rare:161 | ||||
| chr16:2459909-2460152 | Common:1; Rare:80 |