| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46797506-46797661 | Common:3; Rare:22 | ||||
| chr13:48001220-48001560 | Common:4; Rare:140; Clinvar:3; Clinvar (benign):7 | ||||
| chr13:48037375-48037839 | Common:4; Rare:177; Clinvar:2 | ||||
| chr13:48037892-48038207 | Common:6; Rare:100 | ||||
| chr13:48095001-48095294 | Common:2; Rare:142 | ||||
| chr13:48232958-48233424 | Common:4; Rare:147 | ||||
| chr13:48233549-48233667 | Common:1; Rare:31 | ||||
| chr13:48303414-48303483 | Rare:17 | ||||
| chr13:48303567-48303898 | Rare:104; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48303992-48304048 | Rare:11; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr13:48532589-48532910 | Common:3; Rare:115 | ||||
| chr13:48533045-48533192 | Common:1; Rare:45 | ||||
| chr13:48975566-48975734 | Rare:47 | ||||
| chr13:48975748-48976044 | Common:2; Rare:89 | ||||
| chr13:48976073-48976198 | Rare:37 |