| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:106568067-106568286 | Rare:66 | ||||
| chr13:108215482-108215747 | Common:1; Rare:70 | ||||
| chr13:108218144-108218592 | Common:3; Rare:144 | ||||
| chr13:109786497-109786902 | Common:1; Rare:143 | ||||
| chr13:109786978-109787109 | Common:2; Rare:51 | ||||
| chr13:110507146-110507522 | Common:1; Rare:79 | ||||
| chr13:110561134-110561241 | Common:1; Rare:27 | ||||
| chr13:110561320-110561497 | Common:1; Rare:63 | ||||
| chr13:110561591-110562011 | Common:6; Rare:134 | ||||
| chr13:110562100-110562222 | Rare:27 | ||||
| chr13:110615361-110615773 | Common:2; Rare:147 | ||||
| chr13:110615778-110616008 | Common:3; Rare:66 | ||||
| chr13:110616105-110616454 | Common:4; Rare:83 | ||||
| chr13:110705956-110706514 | Common:5; Rare:185; Clinvar:4; Clinvar (benign):9 | ||||
| chr13:110712117-110712229 | Common:1; Rare:25 |