| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49918378-49918675 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr22:50185690-50185949 | Common:4; Rare:109 | ||||
| chr22:50281645-50281856 | Common:2; Rare:69 | ||||
| chr22:50532494-50532655 | Common:2; Rare:41 | ||||
| chr22:50582784-50583120 | Common:7; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50783570-50783859 | Common:2; Rare:97 | ||||
| chr3:2098616-2098936 | Common:4; Rare:125 | ||||
| chr3:3126813-3127016 | Common:4; Rare:93; Clinvar (benign):4 | ||||
| chr3:4303252-4303399 | Common:1; Rare:55 | ||||
| chr3:4493177-4493348 | Rare:60 | ||||
| chr3:4813948-4814224 | Common:3; Rare:61 | ||||
| chr3:4814417-4814676 | Common:5; Rare:82; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:4979747-4979806 | Rare:14 | ||||
| chr3:4980376-4980591 | Common:1; Rare:59 | ||||
| chr3:8501536-8501969 | Common:3; Rare:156 |