| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:100674745-100675234 | Common:6; Rare:203 | ||||
| chr13:102596183-102596528 | Common:2; Rare:58 | ||||
| chr13:102596665-102597045 | Common:1; Rare:156; Clinvar (benign):1 | ||||
| chr13:102772998-102773166 | Common:1; Rare:30 | ||||
| chr13:102773565-102774014 | Common:3; Rare:148 | ||||
| chr13:102798844-102799398 | Common:3; Rare:114 | ||||
| chr13:102800225-102800459 | Common:1; Rare:63 | ||||
| chr13:102800775-102800916 | Common:1; Rare:32 | ||||
| chr13:102845675-102846129 | Common:9; Rare:123; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:102846427-102846919 | Common:2; Rare:102 | ||||
| chr13:106535595-106535869 | Common:2; Rare:109 | ||||
| chr13:106561921-106562030 | Common:1; Rare:23 | ||||
| chr13:106567199-106567574 | Common:2; Rare:99 | ||||
| chr13:106567616-106567748 | Rare:44 | ||||
| chr13:106568052-106568350 | Common:2; Rare:84 |