| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7561784-7561991 | Common:2; Rare:58 | ||||
| chr17:7577078-7577363 | Common:1; Rare:73 | ||||
| chr17:7579356-7579722 | Common:1; Rare:122 | ||||
| chr17:7580198-7580504 | Common:1; Rare:90 | ||||
| chr17:7580521-7580782 | Common:1; Rare:96 | ||||
| chr17:7583508-7583865 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7627361-7627633 | Common:1; Rare:85 | ||||
| chr17:7627635-7627994 | Common:3; Rare:125 | ||||
| chr17:7686418-7686677 | Rare:64 | ||||
| chr17:7687471-7687574 | Rare:25 | ||||
| chr17:7843672-7843774 | Rare:39 | ||||
| chr17:7857170-7857656 | Common:3; Rare:206 | ||||
| chr17:7885200-7885346 | Rare:42 | ||||
| chr17:7931890-7932258 | Common:5; Rare:99 | ||||
| chr17:8147555-8147595 | Rare:17 |