| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99086670-99086798 | Common:2; Rare:50 | ||||
| chr13:99200605-99200931 | Common:7; Rare:144 | ||||
| chr13:99201410-99201700 | Common:1; Rare:100 | ||||
| chr13:99307391-99307505 | Rare:14 | ||||
| chr13:99501193-99501527 | Common:1; Rare:100 | ||||
| chr13:99606437-99606785 | Common:6; Rare:125 | ||||
| chr13:100088848-100089170 | Rare:125; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:100674776-100675095 | Common:4; Rare:135 | ||||
| chr13:102402358-102402554 | Rare:41 | ||||
| chr13:102596487-102596638 | Rare:26 | ||||
| chr13:102596760-102597013 | Common:1; Rare:105 | ||||
| chr13:102773726-102773904 | Common:1; Rare:80 | ||||
| chr13:102798891-102799124 | Common:1; Rare:50 | ||||
| chr13:102800120-102800820 | Common:4; Rare:170 | ||||
| chr13:102845686-102845901 | Common:6; Rare:68; Clinvar (benign):3 |