| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48037592-48037789 | Common:1; Rare:85 | ||||
| chr13:48233064-48233475 | Common:3; Rare:143 | ||||
| chr13:48303665-48304024 | Common:1; Rare:122; Clinvar:14; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr13:48492651-48492756 | Rare:28 | ||||
| chr13:48533038-48533223 | Common:2; Rare:57 | ||||
| chr13:48975757-48975932 | Common:2; Rare:58 | ||||
| chr13:48976410-48976828 | Common:3; Rare:131 | ||||
| chr13:49197551-49197861 | Common:1; Rare:62 | ||||
| chr13:49247777-49247976 | Rare:53 | ||||
| chr13:49443996-49444507 | Common:2; Rare:159 | ||||
| chr13:49495921-49496175 | Common:3; Rare:65 | ||||
| chr13:49585466-49585633 | Common:1; Rare:55 | ||||
| chr13:49936240-49936574 | Common:1; Rare:100 | ||||
| chr13:50081952-50082354 | Common:1; Rare:113 | ||||
| chr13:50909563-50909775 | Common:1; Rare:44; Clinvar:2 |