| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45051453-45051669 | Common:1; Rare:77 | ||||
| chr17:45060987-45061347 | Common:2; Rare:98 | ||||
| chr17:45148160-45148615 | Common:1; Rare:158 | ||||
| chr17:45161494-45161788 | Common:1; Rare:76 | ||||
| chr17:45262092-45262205 | Common:1; Rare:15 | ||||
| chr17:45894247-45894579 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:46193517-46193613 | Common:1; Rare:32 | ||||
| chr17:46922856-46923187 | Common:4; Rare:92; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189202-47189446 | Common:1; Rare:70 | ||||
| chr17:47323868-47323987 | Common:1; Rare:39 | ||||
| chr17:47649598-47649965 | Common:1; Rare:138 | ||||
| chr17:47831503-47831631 | Rare:35 | ||||
| chr17:47895940-47896274 | Rare:107 | ||||
| chr17:47896480-47896565 | Rare:20 | ||||
| chr17:47941354-47941732 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 |