| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:43879458-43879624 | Rare:44 | ||||
| chr13:43879684-43879913 | Common:18; Rare:65 | ||||
| chr13:44436760-44436997 | Common:2; Rare:73 | ||||
| chr13:44989410-44989641 | Rare:99 | ||||
| chr13:45120373-45120720 | Common:5; Rare:108 | ||||
| chr13:45206392-45206703 | Common:2; Rare:48 | ||||
| chr13:45341040-45341609 | Common:4; Rare:258 | ||||
| chr13:46052718-46052867 | Common:2; Rare:41 | ||||
| chr13:46797094-46797261 | Common:2; Rare:56 | ||||
| chr13:48001246-48001405 | Common:1; Rare:74; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037914-48038140 | Common:5; Rare:69 | ||||
| chr13:48303674-48303904 | Rare:78; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48975800-48975928 | Rare:48 | ||||
| chr13:48976297-48976662 | Common:3; Rare:117 | ||||
| chr13:49110228-49110404 | Common:2; Rare:49 |