| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:79481166-79481467 | Common:1; Rare:129 | ||||
| chr13:80338896-80339250 | Common:1; Rare:77 | ||||
| chr13:80339609-80339736 | Rare:28 | ||||
| chr13:80341288-80341478 | Rare:60 | ||||
| chr13:83882283-83882453 | Rare:40; Clinvar:1 | ||||
| chr13:93226791-93227439 | Common:2; Rare:142; Clinvar:7; Clinvar (benign):2 | ||||
| chr13:94596119-94596334 | Common:2; Rare:75 | ||||
| chr13:94601581-94601930 | Common:4; Rare:105 | ||||
| chr13:95552577-95552751 | Common:1; Rare:59 | ||||
| chr13:95676828-95677192 | Common:3; Rare:140 | ||||
| chr13:96053336-96053477 | Common:1; Rare:64 | ||||
| chr13:97222190-97222405 | Rare:35 | ||||
| chr13:97434614-97434689 | Rare:11 | ||||
| chr13:99200668-99200900 | Common:6; Rare:109 | ||||
| chr13:99307337-99307457 | Rare:15 |