| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:79406210-79406339 | Common:3; Rare:40 | ||||
| chr13:79480986-79481463 | Common:2; Rare:183 | ||||
| chr13:85799292-85799517 | Common:2; Rare:37 | ||||
| chr13:91398481-91398690 | Common:2; Rare:73 | ||||
| chr13:93226668-93227107 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:93227286-93227439 | Rare:41; Clinvar:5 | ||||
| chr13:94596106-94596369 | Common:2; Rare:92 | ||||
| chr13:94601596-94601989 | Common:3; Rare:125 | ||||
| chr13:95676819-95677238 | Common:5; Rare:166 | ||||
| chr13:96053209-96053594 | Common:2; Rare:157 | ||||
| chr13:97222137-97222415 | Rare:49 | ||||
| chr13:97433925-97434207 | Common:1; Rare:109 | ||||
| chr13:97976440-97976773 | Common:1; Rare:123 | ||||
| chr13:99200648-99200921 | Common:7; Rare:126 | ||||
| chr13:100088849-100089139 | Rare:111; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |