| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:20525796-20525940 | Common:1; Rare:59 | ||||
| chr13:21140408-21140636 | Rare:106 | ||||
| chr13:21176473-21176717 | Common:2; Rare:111 | ||||
| chr13:24160581-24160764 | Rare:54 | ||||
| chr13:24512704-24512843 | Common:3; Rare:38 | ||||
| chr13:24922796-24923024 | Common:1; Rare:68; Clinvar:1 | ||||
| chr13:25301502-25301700 | Common:1; Rare:78 | ||||
| chr13:26221787-26221970 | Rare:51 | ||||
| chr13:26222243-26222375 | Common:2; Rare:38 | ||||
| chr13:27251251-27251632 | Common:5; Rare:115 | ||||
| chr13:27450130-27450240 | Common:3; Rare:35 | ||||
| chr13:27450507-27450621 | Common:2; Rare:52 | ||||
| chr13:28658868-28659194 | Common:1; Rare:124; Clinvar (pathogenic):1 | ||||
| chr13:30306813-30307197 | Common:7; Rare:102 | ||||
| chr13:30617526-30617908 | Common:1; Rare:132 |