| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47253690-47253878 | Common:3; Rare:50; Clinvar (benign):1 | ||||
| chr17:47323464-47323797 | Common:4; Rare:73 | ||||
| chr17:47323856-47324052 | Common:3; Rare:74 | ||||
| chr17:47522970-47523063 | Rare:18 | ||||
| chr17:47592227-47592525 | Common:1; Rare:49 | ||||
| chr17:47649302-47649479 | Rare:52 | ||||
| chr17:47649534-47650435 | Common:1; Rare:321 | ||||
| chr17:47694623-47694832 | Common:3; Rare:46 | ||||
| chr17:47831507-47831731 | Rare:63 | ||||
| chr17:47841216-47841366 | Rare:31 | ||||
| chr17:47895917-47896274 | Rare:117 | ||||
| chr17:47896476-47896578 | Rare:24 | ||||
| chr17:47941328-47941786 | Rare:119; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr17:47967670-47967877 | Common:4; Rare:27 | ||||
| chr17:47970920-47971157 | Common:1; Rare:58 |