| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99200223-99200337 | Rare:26 | ||||
| chr13:99200433-99200959 | Common:8; Rare:200 | ||||
| chr13:99501193-99501521 | Common:1; Rare:99 | ||||
| chr13:99501738-99501769 | Rare:14 | ||||
| chr13:99606555-99606864 | Common:4; Rare:126 | ||||
| chr13:99606883-99606944 | Rare:20 | ||||
| chr13:99971516-99972103 | Common:6; Rare:164; Clinvar:1 | ||||
| chr13:99981010-99981388 | Rare:109 | ||||
| chr13:99981492-99981922 | Common:1; Rare:143 | ||||
| chr13:99982166-99982468 | Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:99984229-99984472 | Common:3; Rare:43 | ||||
| chr13:99984808-99985048 | Common:1; Rare:52 | ||||
| chr13:100088905-100089147 | Rare:93; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr13:100306049-100306321 | Rare:44 | ||||
| chr13:100514960-100515098 | Rare:27 |