| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:44435144-44435447 | Common:3; Rare:88 | ||||
| chr13:44436783-44437028 | Common:2; Rare:76 | ||||
| chr13:44989441-44989610 | Rare:63 | ||||
| chr13:45120363-45120532 | Common:2; Rare:47 | ||||
| chr13:45341036-45341609 | Common:4; Rare:259 | ||||
| chr13:45418340-45418539 | Rare:58 | ||||
| chr13:46052696-46052850 | Common:2; Rare:42 | ||||
| chr13:48037513-48037759 | Rare:96 | ||||
| chr13:48233046-48233475 | Common:5; Rare:147 | ||||
| chr13:48303674-48303897 | Rare:74; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48975703-48975923 | Common:2; Rare:66 | ||||
| chr13:49247807-49247964 | Rare:41 | ||||
| chr13:49444005-49444476 | Common:1; Rare:152 | ||||
| chr13:49495902-49496063 | Rare:35 | ||||
| chr13:49585524-49585612 | Common:1; Rare:27 |