| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:41457261-41457551 | Common:2; Rare:79 | ||||
| chr13:43879492-43879881 | Common:19; Rare:108 | ||||
| chr13:44989443-44989597 | Rare:58 | ||||
| chr13:45120254-45120580 | Common:2; Rare:82 | ||||
| chr13:45341040-45341617 | Common:4; Rare:259 | ||||
| chr13:46052696-46052819 | Common:2; Rare:36 | ||||
| chr13:48037615-48037783 | Common:1; Rare:75 | ||||
| chr13:48037923-48038052 | Common:4; Rare:42 | ||||
| chr13:48233059-48233222 | Common:1; Rare:54 | ||||
| chr13:48303674-48303885 | Rare:71; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48975622-48975928 | Common:2; Rare:94 | ||||
| chr13:48976768-48976891 | Rare:27 | ||||
| chr13:49247807-49247976 | Rare:48 | ||||
| chr13:49444005-49444530 | Common:2; Rare:163 | ||||
| chr13:49495942-49496029 | Rare:24 |