| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:46225353-46225481 | Common:1; Rare:34 | ||||
| chr17:46922869-46923216 | Common:4; Rare:105; Clinvar:4; Clinvar (benign):9 | ||||
| chr17:47189235-47189568 | Rare:84 | ||||
| chr17:47253689-47253859 | Common:3; Rare:44; Clinvar (benign):1 | ||||
| chr17:47323890-47323998 | Common:1; Rare:31 | ||||
| chr17:47530957-47531286 | Common:1; Rare:86 | ||||
| chr17:47649518-47650399 | Common:1; Rare:320 | ||||
| chr17:47679849-47680103 | Common:1; Rare:55 | ||||
| chr17:47831501-47831751 | Rare:71 | ||||
| chr17:47895958-47896269 | Rare:94 | ||||
| chr17:47941356-47941732 | Rare:102; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:47970762-47971092 | Common:4; Rare:70 | ||||
| chr17:48048069-48048434 | Rare:95 | ||||
| chr17:48048625-48048897 | Common:3; Rare:48 | ||||
| chr17:48107437-48107831 | Common:5; Rare:95 |