| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:20900047-20900750 | Common:5; Rare:151 | ||||
| chr16:20900761-20900840 | Common:1; Rare:29 | ||||
| chr16:21953038-21953413 | Common:1; Rare:96; Clinvar (benign):3 | ||||
| chr16:22436939-22437071 | Rare:51 | ||||
| chr16:22437162-22437308 | Rare:45 | ||||
| chr16:23452741-23452794 | Rare:19 | ||||
| chr16:23453163-23453220 | Rare:16 | ||||
| chr16:23641247-23641543 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
| chr16:25111472-25111817 | Common:2; Rare:96 | ||||
| chr16:27268719-27268912 | Common:1; Rare:70 | ||||
| chr16:27313789-27313993 | Common:2; Rare:58 | ||||
| chr16:27549882-27550167 | Common:2; Rare:107 | ||||
| chr16:28822549-28822732 | Rare:65 | ||||
| chr16:28846246-28846623 | Common:2; Rare:132; Clinvar:6; Clinvar (benign):6 | ||||
| chr16:28863721-28863848 | Common:1; Rare:38 |