| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:20703340-20703820 | Common:6; Rare:264 | ||||
| chr13:20703979-20704750 | Common:4; Rare:328 | ||||
| chr13:20773804-20774095 | Common:2; Rare:192 | ||||
| chr13:20902631-20903030 | Common:3; Rare:243 | ||||
| chr13:20903033-20903420 | Common:1; Rare:173 | ||||
| chr13:21061176-21061319 | Rare:38 | ||||
| chr13:21061447-21061761 | Common:2; Rare:157 | ||||
| chr13:21140110-21140964 | Common:2; Rare:640 | ||||
| chr13:21175965-21176430 | Common:10; Rare:254 | ||||
| chr13:21176456-21176997 | Common:14; Rare:557 | ||||
| chr13:21459086-21459545 | Common:4; Rare:377 | ||||
| chr13:21603692-21603998 | Rare:280 | ||||
| chr13:21603965-21604338 | Common:13; Rare:354 | ||||
| chr13:21670941-21671134 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr13:23375331-23375823 | Common:11; Rare:279 |