| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:100588590-100588812 | Common:5; Rare:74 | ||||
| chr13:100674347-100674492 | Common:1; Rare:50 | ||||
| chr13:100674735-100675203 | Common:6; Rare:197 | ||||
| chr13:102596462-102596541 | Rare:14 | ||||
| chr13:102596668-102597074 | Common:1; Rare:160; Clinvar (benign):1 | ||||
| chr13:102773367-102773396 | Rare:7 | ||||
| chr13:102773541-102773584 | Rare:13 | ||||
| chr13:102773652-102773958 | Common:1; Rare:116 | ||||
| chr13:102798912-102799339 | Common:1; Rare:84 | ||||
| chr13:102800056-102800473 | Common:2; Rare:101 | ||||
| chr13:102845647-102845963 | Common:6; Rare:88; Clinvar (benign):3 | ||||
| chr13:102845988-102846116 | Common:3; Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:102846528-102846867 | Common:2; Rare:74 | ||||
| chr13:106535612-106536089 | Common:3; Rare:169 | ||||
| chr13:106567208-106567288 | Rare:23 |