| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:51584208-51584592 | Common:4; Rare:127 | ||||
| chr13:51584746-51585434 | Common:2; Rare:298 | ||||
| chr13:51803669-51803862 | Rare:57 | ||||
| chr13:51803920-51804400 | Common:2; Rare:138 | ||||
| chr13:52012110-52012495 | Common:2; Rare:148; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:52159506-52159635 | Common:1; Rare:37 | ||||
| chr13:52449770-52450160 | Common:1; Rare:90 | ||||
| chr13:52450576-52450852 | Rare:79 | ||||
| chr13:52455240-52455523 | Common:3; Rare:92 | ||||
| chr13:52652267-52652475 | Common:3; Rare:60 | ||||
| chr13:52652562-52652927 | Common:3; Rare:112 | ||||
| chr13:52848611-52848762 | Common:2; Rare:44 | ||||
| chr13:57631474-57631874 | Common:6; Rare:200 | ||||
| chr13:57632204-57632761 | Common:4; Rare:272 | ||||
| chr13:60163877-60164197 | Common:1; Rare:88 |