| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49495707-49496055 | Rare:85 | ||||
| chr13:49521836-49522008 | Common:2; Rare:45 | ||||
| chr13:49585491-49585612 | Common:1; Rare:40 | ||||
| chr13:49792502-49792811 | Common:5; Rare:124 | ||||
| chr13:49936199-49936601 | Common:1; Rare:126 | ||||
| chr13:49996699-49997099 | Common:1; Rare:96 | ||||
| chr13:50081951-50082341 | Common:1; Rare:110 | ||||
| chr13:50715471-50715690 | Rare:50 | ||||
| chr13:50909706-50910074 | Common:1; Rare:80; Clinvar:5; Clinvar (benign):1 | ||||
| chr13:51451136-51451264 | Rare:21 | ||||
| chr13:51452240-51452520 | Rare:70 | ||||
| chr13:51452533-51452655 | Common:1; Rare:51 | ||||
| chr13:51452993-51453388 | Rare:158 | ||||
| chr13:51584403-51584561 | Common:1; Rare:59 | ||||
| chr13:51804094-51804227 | Common:2; Rare:42 |