| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7354511-7354911 | Common:1; Rare:115 | ||||
| chr17:7394518-7394727 | Common:2; Rare:62 | ||||
| chr17:7394940-7395290 | Rare:55 | ||||
| chr17:7403732-7403872 | Common:5; Rare:37 | ||||
| chr17:7404034-7404243 | Rare:82 | ||||
| chr17:7404453-7404670 | Common:2; Rare:63 | ||||
| chr17:7404744-7404921 | Common:4; Rare:42 | ||||
| chr17:7438001-7438501 | Common:2; Rare:275 | ||||
| chr17:7439774-7440317 | Common:1; Rare:158 | ||||
| chr17:7440446-7440750 | Rare:60 | ||||
| chr17:7445397-7445566 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr17:7455340-7455900 | Common:5; Rare:169; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:7483820-7484087 | Common:5; Rare:61 | ||||
| chr17:7484237-7484414 | Common:2; Rare:90 | ||||
| chr17:7484666-7484842 | Rare:75 |