| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:19804699-19804949 | Common:3; Rare:123 | ||||
| chr6:19866287-19866540 | Common:1; Rare:39 | ||||
| chr6:21521271-21521850 | Common:1; Rare:104 | ||||
| chr6:21522102-21522230 | Common:1; Rare:20 | ||||
| chr6:21522482-21522611 | Rare:26 | ||||
| chr6:21523196-21523277 | Rare:10 | ||||
| chr6:21587260-21587447 | Common:2; Rare:31 | ||||
| chr6:21587863-21588463 | Common:3; Rare:113 | ||||
| chr6:21588911-21589061 | Common:2; Rare:22 | ||||
| chr6:21593519-21593907 | Common:1; Rare:97 | ||||
| chr6:21593909-21594122 | Common:1; Rare:42 | ||||
| chr6:21594453-21594784 | Common:2; Rare:89; Clinvar (pathogenic):1 | ||||
| chr6:21594902-21595033 | Rare:45 | ||||
| chr6:21595597-21596216 | Common:3; Rare:246 | ||||
| chr6:21596295-21596787 | Common:2; Rare:171 |