| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:44435170-44435448 | Common:3; Rare:79 | ||||
| chr13:44436760-44437033 | Common:2; Rare:85 | ||||
| chr13:44989443-44989607 | Rare:62 | ||||
| chr13:45120373-45120565 | Common:2; Rare:63 | ||||
| chr13:45341040-45341525 | Common:4; Rare:233 | ||||
| chr13:46052709-46052847 | Common:2; Rare:35 | ||||
| chr13:46211814-46211935 | Common:1; Rare:42 | ||||
| chr13:46553056-46553210 | Common:2; Rare:55 | ||||
| chr13:46797112-46797326 | Common:3; Rare:78 | ||||
| chr13:46896845-46896971 | Rare:34 | ||||
| chr13:48001253-48001397 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):3 | ||||
| chr13:48037683-48037775 | Rare:48 | ||||
| chr13:48233101-48233183 | Rare:17 | ||||
| chr13:48975810-48975932 | Rare:45 | ||||
| chr13:49247844-49247977 | Rare:43 |