| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48001209-48001217 | Rare:2 | ||||
| chr13:48001238-48001418 | Common:1; Rare:83; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037648-48037782 | Rare:65 | ||||
| chr13:48037929-48038141 | Common:5; Rare:62 | ||||
| chr13:48094963-48095035 | Rare:27 | ||||
| chr13:48303671-48304032 | Common:1; Rare:121; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr13:48976478-48976662 | Common:2; Rare:62 | ||||
| chr13:49247830-49248092 | Rare:80 | ||||
| chr13:49443984-49444335 | Common:1; Rare:116 | ||||
| chr13:49585482-49585629 | Common:1; Rare:47 | ||||
| chr13:49691286-49691413 | Rare:46 | ||||
| chr13:49706158-49706352 | Rare:47 | ||||
| chr13:49792481-49792605 | Common:3; Rare:74 | ||||
| chr13:49936188-49936204 | Rare:3 | ||||
| chr13:49936226-49936585 | Common:1; Rare:108 |