| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48303674-48304029 | Common:1; Rare:120; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr13:48533046-48533110 | Common:1; Rare:20 | ||||
| chr13:48975800-48975961 | Rare:59 | ||||
| chr13:48976017-48976123 | Rare:34 | ||||
| chr13:48976340-48976831 | Common:3; Rare:148 | ||||
| chr13:49247795-49248035 | Rare:65 | ||||
| chr13:49248314-49248617 | Rare:43 | ||||
| chr13:49443997-49444477 | Common:1; Rare:156 | ||||
| chr13:49495551-49495750 | Rare:42 | ||||
| chr13:49495922-49496078 | Rare:39 | ||||
| chr13:49585461-49585658 | Common:1; Rare:70 | ||||
| chr13:49936260-49936587 | Common:1; Rare:100 | ||||
| chr13:49996759-49997089 | Common:1; Rare:63 | ||||
| chr13:50081951-50082262 | Common:1; Rare:86 | ||||
| chr13:50715517-50715690 | Rare:33 |