| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:76885053-76885343 | Common:1; Rare:99 | ||||
| chr13:76885349-76885602 | Common:1; Rare:88 | ||||
| chr13:87671289-87671401 | Rare:35 | ||||
| chr13:94549373-94549457 | Common:1; Rare:26 | ||||
| chr13:99087946-99087983 | Rare:9 | ||||
| chr13:102394493-102394654 | Common:1; Rare:60 | ||||
| chr13:109781742-109781862 | Common:1; Rare:29 | ||||
| chr13:109784412-109784491 | Rare:33 | ||||
| chr13:110182991-110183187 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr13:110307843-110308102 | Common:1; Rare:99 | ||||
| chr13:110308515-110308622 | Common:1; Rare:21 | ||||
| chr13:110340908-110341212 | Common:3; Rare:68 | ||||
| chr13:110388286-110388605 | Common:4; Rare:60 | ||||
| chr13:110416327-110416443 | Common:1; Rare:11 | ||||
| chr13:110424829-110424993 | Common:4; Rare:56; Clinvar:3; Clinvar (benign):2 |