| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32428122-32428199 | Rare:14 | ||||
| chr13:32586234-32586582 | Common:2; Rare:104 | ||||
| chr13:33350561-33350811 | Rare:68 | ||||
| chr13:33817994-33818222 | Common:1; Rare:104 | ||||
| chr13:35476647-35476809 | Common:1; Rare:25 | ||||
| chr13:36297787-36297923 | Rare:50 | ||||
| chr13:36345559-36345657 | Common:1; Rare:19 | ||||
| chr13:36346294-36346457 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36999251-36999448 | Rare:79 | ||||
| chr13:37000246-37000407 | Common:2; Rare:30 | ||||
| chr13:37000744-37000821 | Rare:33; Clinvar (pathogenic):1 | ||||
| chr13:37059585-37059741 | Common:1; Rare:53 | ||||
| chr13:39038064-39038460 | Common:1; Rare:95 | ||||
| chr13:39603116-39603303 | Common:1; Rare:63 | ||||
| chr13:39655619-39655759 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 |