| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132956786-132956920 | Rare:14 | ||||
| chr12:133038729-133039026 | Common:3; Rare:49 | ||||
| chr12:133040573-133040665 | Rare:6 | ||||
| chr12:133080180-133080483 | Common:8; Rare:95 | ||||
| chr12:133130234-133130667 | Common:7; Rare:145 | ||||
| chr13:19633858-19633959 | Rare:34 | ||||
| chr13:19782876-19783249 | Common:2; Rare:110 | ||||
| chr13:19863420-19863866 | Common:5; Rare:153 | ||||
| chr13:19958432-19959075 | Common:9; Rare:268 | ||||
| chr13:20024308-20024641 | Common:1; Rare:59 | ||||
| chr13:20024645-20024841 | Common:1; Rare:34 | ||||
| chr13:20192783-20193012 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):3 | ||||
| chr13:20525778-20525936 | Common:1; Rare:66 | ||||
| chr13:20773923-20774064 | Common:1; Rare:44 | ||||
| chr13:20902709-20902882 | Common:1; Rare:50 |