| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7583535-7583858 | Common:1; Rare:131; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:7584070-7584122 | Rare:11 | ||||
| chr17:7857170-7857409 | Common:2; Rare:119 | ||||
| chr17:7885200-7885340 | Rare:41 | ||||
| chr17:7885506-7885662 | Rare:32 | ||||
| chr17:7931895-7932248 | Common:5; Rare:95 | ||||
| chr17:8150713-8151028 | Common:3; Rare:95 | ||||
| chr17:8151256-8151491 | Common:2; Rare:53 | ||||
| chr17:8152348-8152567 | Common:2; Rare:51 | ||||
| chr17:8162926-8163099 | Rare:60 | ||||
| chr17:8176331-8176483 | Rare:46 | ||||
| chr17:8248042-8248098 | Rare:32; Clinvar:2 | ||||
| chr17:8249226-8249319 | Common:1; Rare:28 | ||||
| chr17:8310761-8310822 | Rare:22 | ||||
| chr17:8376656-8376786 | Common:1; Rare:55 |