| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:77877-78340 | Common:29; Rare:629 | ||||
| chr16:119840-120340 | Common:13; Rare:253 | ||||
| chr16:137907-138307 | Common:2; Rare:201; Clinvar:5; Clinvar (benign):2 | ||||
| chr16:138280-139615 | Common:113; Rare:936 | ||||
| chr16:152270-153425 | Common:26; Rare:543 | ||||
| chr16:175638-177263 | Common:17; Rare:380; Clinvar:14; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr16:180120-180564 | Common:10; Rare:345 | ||||
| chr16:228343-228933 | Rare:161 | ||||
| chr16:229091-229245 | Common:6; Rare:203 | ||||
| chr16:229292-229692 | Common:8; Rare:296 | ||||
| chr16:234268-234682 | Common:4; Rare:304 | ||||
| chr16:234587-235280 | Common:7; Rare:704 | ||||
| chr16:280100-280652 | Common:6; Rare:172 | ||||
| chr16:351713-353277 | Common:39; Rare:1076 | ||||
| chr16:369138-369781 | Common:25; Rare:598 |