| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:40767014-40767291 | Common:3; Rare:58 | ||||
| chr13:40813109-40813119 | Common:3 | ||||
| chr13:40874226-40874502 | Common:5; Rare:65 | ||||
| chr13:40921658-40921927 | Common:5; Rare:72 | ||||
| chr13:41192899-41193192 | Rare:71; Clinvar (benign):1 | ||||
| chr13:41383697-41383731 | Rare:3 | ||||
| chr13:41569666-41569894 | Common:2; Rare:42 | ||||
| chr13:41664528-41664626 | Common:1; Rare:16 | ||||
| chr13:41875945-41876053 | Rare:19 | ||||
| chr13:42047856-42048077 | Rare:56 | ||||
| chr13:42076383-42076685 | Common:2; Rare:62 | ||||
| chr13:42087179-42087485 | Common:2; Rare:48 | ||||
| chr13:42091121-42091387 | Rare:41 | ||||
| chr13:42091761-42091915 | Common:1; Rare:21 | ||||
| chr13:42092297-42092614 | Common:1; Rare:61 |