| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39602686-39602834 | Rare:45 | ||||
| chr13:39603109-39603359 | Common:2; Rare:87 | ||||
| chr13:39655545-39655801 | Common:4; Rare:128; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:39655841-39655854 | Rare:6; Clinvar (benign):1 | ||||
| chr13:40666425-40667064 | Common:3; Rare:201 | ||||
| chr13:40771092-40771507 | Common:3; Rare:128 | ||||
| chr13:40789312-40789855 | Common:3; Rare:176; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:40982969-40983039 | Common:1; Rare:12 | ||||
| chr13:41019060-41019136 | Rare:9 | ||||
| chr13:41019250-41019463 | Rare:33 | ||||
| chr13:41060012-41060570 | Common:4; Rare:190 | ||||
| chr13:41060795-41061188 | Common:18; Rare:202 | ||||
| chr13:41061215-41061957 | Common:4; Rare:263 | ||||
| chr13:41132466-41133074 | Common:3; Rare:170 | ||||
| chr13:41194339-41194743 | Common:2; Rare:90 |