| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:38350215-38350287 | Rare:37 | ||||
| chr13:38686745-38687129 | Common:5; Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:39037795-39038056 | Common:1; Rare:85 | ||||
| chr13:39038087-39038484 | Common:1; Rare:98 | ||||
| chr13:39603128-39603272 | Common:1; Rare:52 | ||||
| chr13:39655836-39655895 | Rare:23; Clinvar (benign):2 | ||||
| chr13:40771063-40771356 | Common:3; Rare:106 | ||||
| chr13:40789347-40789615 | Common:2; Rare:90; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41060868-41061027 | Common:16; Rare:100 | ||||
| chr13:41061140-41061657 | Common:4; Rare:176 | ||||
| chr13:41061741-41061839 | Common:1; Rare:33 | ||||
| chr13:41132732-41133002 | Rare:72 | ||||
| chr13:41194466-41194685 | Common:2; Rare:47 | ||||
| chr13:41311147-41311337 | Common:1; Rare:79 | ||||
| chr13:42271758-42272190 | Common:4; Rare:114 |