| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27620527-27620966 | Common:4; Rare:146 | ||||
| chr13:27621065-27621485 | Common:4; Rare:112 | ||||
| chr13:27945418-27945565 | Common:1; Rare:38 | ||||
| chr13:28137999-28138588 | Common:4; Rare:164 | ||||
| chr13:28138973-28139086 | Rare:28 | ||||
| chr13:28658864-28659001 | Common:1; Rare:30 | ||||
| chr13:28659068-28659187 | Rare:51; Clinvar (pathogenic):1 | ||||
| chr13:28659515-28659728 | Common:1; Rare:50 | ||||
| chr13:28718864-28719189 | Common:1; Rare:86 | ||||
| chr13:29586712-29586862 | Rare:23 | ||||
| chr13:29595382-29595599 | Common:2; Rare:60 | ||||
| chr13:29595603-29595879 | Common:2; Rare:96 | ||||
| chr13:30307001-30307204 | Common:4; Rare:49 | ||||
| chr13:30307361-30307575 | Common:2; Rare:75 | ||||
| chr13:30464612-30464820 | Common:1; Rare:75 |