| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:133080679-133080970 | Common:2; Rare:94 | ||||
| chr12:133130232-133130662 | Common:7; Rare:144 | ||||
| chr12:133181364-133181567 | Common:2; Rare:61 | ||||
| chr13:19633355-19633746 | Common:1; Rare:143 | ||||
| chr13:19782912-19783090 | Common:2; Rare:64 | ||||
| chr13:19863441-19863947 | Common:6; Rare:181 | ||||
| chr13:20160939-20161126 | Rare:64; Clinvar (benign):1 | ||||
| chr13:20161530-20161704 | Common:1; Rare:49 | ||||
| chr13:20525784-20525968 | Common:1; Rare:71 | ||||
| chr13:20566811-20567219 | Common:1; Rare:120 | ||||
| chr13:20773925-20774042 | Rare:38 | ||||
| chr13:21061513-21061722 | Common:1; Rare:64 | ||||
| chr13:21140394-21140624 | Rare:106 | ||||
| chr13:21176478-21176724 | Common:2; Rare:110 | ||||
| chr13:21459204-21459521 | Common:1; Rare:115 |