| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:79405791-79405909 | Rare:40 | ||||
| chr13:79406219-79406334 | Common:3; Rare:36 | ||||
| chr13:79481207-79481524 | Common:1; Rare:133 | ||||
| chr13:80338881-80338932 | Rare:5 | ||||
| chr13:80338955-80339126 | Rare:42 | ||||
| chr13:80339167-80339504 | Common:3; Rare:78 | ||||
| chr13:80340824-80341123 | Common:1; Rare:90 | ||||
| chr13:93226705-93227422 | Common:3; Rare:147; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:94596104-94596325 | Common:2; Rare:81 | ||||
| chr13:95301265-95301531 | Common:1; Rare:85 | ||||
| chr13:96013130-96013321 | Common:1; Rare:37 | ||||
| chr13:96053157-96053196 | Rare:12 | ||||
| chr13:96053345-96053526 | Common:2; Rare:84 | ||||
| chr13:97433933-97434197 | Common:1; Rare:104 | ||||
| chr13:97434826-97435085 | Common:2; Rare:57 |