| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:94601592-94602010 | Common:3; Rare:133 | ||||
| chr13:95300895-95301081 | Common:2; Rare:36 | ||||
| chr13:95301344-95301620 | Common:1; Rare:76 | ||||
| chr13:95676819-95677242 | Common:5; Rare:168 | ||||
| chr13:96053209-96053519 | Common:2; Rare:130 | ||||
| chr13:97222190-97222395 | Rare:34 | ||||
| chr13:97434612-97434698 | Rare:13 | ||||
| chr13:99200652-99200933 | Common:7; Rare:130 | ||||
| chr13:99606504-99606715 | Common:5; Rare:68 | ||||
| chr13:100088851-100089117 | Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:100588756-100589079 | Common:2; Rare:74 | ||||
| chr13:100674778-100675156 | Common:4; Rare:157 | ||||
| chr13:102596773-102597039 | Common:1; Rare:122 | ||||
| chr13:102773699-102773869 | Rare:68 | ||||
| chr13:102845714-102846168 | Common:9; Rare:116; Clinvar:4; Clinvar (benign):4 |