| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:84295639-84295666 | Rare:12 | ||||
| chr16:84295803-84296160 | Common:3; Rare:91 | ||||
| chr16:84302946-84303164 | Common:2; Rare:49 | ||||
| chr16:84618692-84618820 | Common:1; Rare:29 | ||||
| chr16:87779079-87779328 | Common:1; Rare:74 | ||||
| chr16:87851785-87851935 | Common:1; Rare:64 | ||||
| chr16:87853733-87853826 | Common:1; Rare:32 | ||||
| chr16:89241022-89241303 | Common:3; Rare:36 | ||||
| chr16:89906163-89906505 | Common:2; Rare:137 | ||||
| chr16:90020695-90020909 | Common:2; Rare:35 | ||||
| chr16:90082033-90082183 | Common:1; Rare:49 | ||||
| chr17:564431-564614 | Common:2; Rare:27 | ||||
| chr17:601486-601642 | Rare:33 | ||||
| chr17:601794-602192 | Common:14; Rare:92; Clinvar (benign):3 | ||||
| chr17:602607-602832 | Common:3; Rare:36 |