| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:44435155-44435463 | Common:3; Rare:91 | ||||
| chr13:44436800-44437017 | Common:2; Rare:67 | ||||
| chr13:44989449-44989607 | Rare:58 | ||||
| chr13:45120392-45120637 | Common:1; Rare:82 | ||||
| chr13:45341036-45341609 | Common:4; Rare:259 | ||||
| chr13:45418340-45418424 | Rare:27 | ||||
| chr13:46052646-46052821 | Common:2; Rare:45 | ||||
| chr13:46387250-46387352 | Rare:26 | ||||
| chr13:46553056-46553399 | Common:4; Rare:101 | ||||
| chr13:48001242-48001405 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037646-48037767 | Rare:56 | ||||
| chr13:48095079-48095215 | Common:1; Rare:61 | ||||
| chr13:48233066-48233222 | Common:1; Rare:53 | ||||
| chr13:48233272-48233475 | Common:2; Rare:68 | ||||
| chr13:48303674-48303897 | Rare:74; Clinvar:3; Clinvar (pathogenic):1 |