| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30464881-30464981 | Common:1; Rare:34 | ||||
| chr13:30617255-30618000 | Common:1; Rare:229 | ||||
| chr13:31138781-31139096 | Common:1; Rare:88 | ||||
| chr13:31161474-31161690 | Common:3; Rare:99 | ||||
| chr13:31161697-31162054 | Common:1; Rare:161 | ||||
| chr13:31162337-31162441 | Common:1; Rare:26 | ||||
| chr13:31199629-31199986 | Common:1; Rare:100 | ||||
| chr13:32315384-32315514 | Common:1; Rare:33 | ||||
| chr13:32522237-32522301 | Common:1; Rare:12 | ||||
| chr13:32586256-32586596 | Common:2; Rare:106 | ||||
| chr13:33284974-33285392 | Common:1; Rare:69 | ||||
| chr13:33285438-33285487 | Rare:8 | ||||
| chr13:33285626-33285954 | Common:2; Rare:82 | ||||
| chr13:36346230-36346525 | Common:3; Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:37000065-37000412 | Common:2; Rare:76 |