| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45341037-45341609 | Common:4; Rare:258 | ||||
| chr13:45418340-45418528 | Rare:54 | ||||
| chr13:46052619-46052856 | Common:2; Rare:58 | ||||
| chr13:46182131-46182449 | Common:3; Rare:52 | ||||
| chr13:46211757-46212009 | Common:2; Rare:74 | ||||
| chr13:46387167-46387332 | Rare:41 | ||||
| chr13:46553056-46553280 | Common:2; Rare:70 | ||||
| chr13:46896824-46897106 | Common:1; Rare:63 | ||||
| chr13:48001242-48001408 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037610-48037820 | Common:2; Rare:95; Clinvar:2 | ||||
| chr13:48233053-48233475 | Common:3; Rare:146 | ||||
| chr13:48975764-48975928 | Common:2; Rare:56 | ||||
| chr13:48976370-48976662 | Common:3; Rare:102 | ||||
| chr13:49247830-49248050 | Rare:64 | ||||
| chr13:49443994-49444477 | Common:1; Rare:156 |