| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7561732-7561996 | Common:2; Rare:81 | ||||
| chr17:7564744-7565041 | Common:2; Rare:87 | ||||
| chr17:7573238-7573530 | Common:4; Rare:99 | ||||
| chr17:7577056-7577487 | Common:1; Rare:104 | ||||
| chr17:7578015-7578550 | Rare:185 | ||||
| chr17:7579377-7579713 | Common:1; Rare:108 | ||||
| chr17:7582856-7583136 | Rare:85 | ||||
| chr17:7583751-7583865 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584084-7584123 | Rare:9 | ||||
| chr17:7627799-7628000 | Common:2; Rare:64 | ||||
| chr17:7650775-7650928 | Common:2; Rare:45 | ||||
| chr17:7674938-7675082 | Rare:39; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):7 | ||||
| chr17:7686397-7686681 | Rare:71 | ||||
| chr17:7687456-7687511 | Rare:13; Clinvar:1 | ||||
| chr17:7687515-7687580 | Rare:15 |