| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32315415-32315536 | Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:33285703-33285896 | Rare:44 | ||||
| chr13:34942160-34942292 | Common:3; Rare:39 | ||||
| chr13:35476323-35476841 | Common:1; Rare:91 | ||||
| chr13:35855549-35855774 | Common:1; Rare:49 | ||||
| chr13:36131374-36131556 | Rare:50 | ||||
| chr13:36346301-36346488 | Common:3; Rare:53; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36673862-36674084 | Common:1; Rare:76 | ||||
| chr13:37000740-37000805 | Rare:26 | ||||
| chr13:37059439-37059754 | Common:1; Rare:90 | ||||
| chr13:37598609-37598721 | Rare:42 | ||||
| chr13:37869734-37869926 | Common:1; Rare:47 | ||||
| chr13:38349522-38349917 | Common:4; Rare:133; Clinvar (pathogenic):1 | ||||
| chr13:38350215-38350287 | Rare:37 | ||||
| chr13:38686871-38687078 | Common:2; Rare:59; Clinvar:1 |