| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46211799-46212009 | Common:2; Rare:65 | ||||
| chr13:46387203-46387357 | Rare:41 | ||||
| chr13:46797098-46797261 | Common:2; Rare:54 | ||||
| chr13:46797673-46797925 | Common:1; Rare:47 | ||||
| chr13:48001237-48001405 | Common:1; Rare:78; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037691-48037775 | Rare:46 | ||||
| chr13:48037931-48038116 | Common:5; Rare:53 | ||||
| chr13:48233066-48233475 | Common:3; Rare:143 | ||||
| chr13:48303683-48303885 | Rare:63; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48492536-48492797 | Common:2; Rare:62 | ||||
| chr13:48533046-48533284 | Common:1; Rare:70 | ||||
| chr13:48975780-48975952 | Common:1; Rare:62 | ||||
| chr13:48976339-48976666 | Common:3; Rare:107 | ||||
| chr13:48976774-48976865 | Rare:22 | ||||
| chr13:49247803-49247976 | Rare:48 |