| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:37105615-37105677 | Common:2; Rare:20 | ||||
| chr13:37570615-37570825 | Common:1; Rare:44 | ||||
| chr13:38349441-38349491 | Rare:12 | ||||
| chr13:38349548-38349917 | Common:3; Rare:126; Clinvar (pathogenic):1 | ||||
| chr13:38350215-38350422 | Rare:66 | ||||
| chr13:38686920-38687109 | Common:2; Rare:47; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:39037714-39037818 | Rare:29 | ||||
| chr13:39038007-39038517 | Common:1; Rare:128 | ||||
| chr13:39038542-39038591 | Rare:14 | ||||
| chr13:39603114-39603284 | Common:1; Rare:56 | ||||
| chr13:39655597-39655809 | Common:3; Rare:105; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40771025-40771355 | Common:3; Rare:115 | ||||
| chr13:40789370-40789609 | Common:2; Rare:79; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:40982877-40983097 | Common:3; Rare:39 | ||||
| chr13:41060493-41060511 | Rare:6 |