| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:41311125-41311336 | Common:1; Rare:84 | ||||
| chr13:42992189-42992372 | Common:2; Rare:36 | ||||
| chr13:43879012-43879136 | Common:1; Rare:27 | ||||
| chr13:43879432-43879614 | Rare:46 | ||||
| chr13:44989467-44989610 | Rare:50 | ||||
| chr13:45340711-45341042 | Common:3; Rare:132 | ||||
| chr13:45341044-45341563 | Common:4; Rare:240 | ||||
| chr13:46182113-46182453 | Common:3; Rare:60 | ||||
| chr13:46387158-46387397 | Common:1; Rare:63 | ||||
| chr13:48037492-48037763 | Rare:104 | ||||
| chr13:48233314-48233468 | Common:2; Rare:56 | ||||
| chr13:48303674-48303893 | Rare:73; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48492545-48492863 | Common:2; Rare:76 | ||||
| chr13:48532994-48533128 | Common:2; Rare:46 | ||||
| chr13:49247830-49248087 | Rare:78 |