| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:40474800-40475062 | Common:1; Rare:46 | ||||
| chr17:40475161-40475176 | Rare:2 | ||||
| chr17:40475179-40475234 | Rare:12 | ||||
| chr17:40475408-40476274 | Common:2; Rare:158 | ||||
| chr17:40481776-40482033 | Common:4; Rare:45 | ||||
| chr17:40482057-40482209 | Rare:51 | ||||
| chr17:40484621-40485034 | Common:1; Rare:95 | ||||
| chr17:40485290-40485551 | Common:2; Rare:41 | ||||
| chr17:40485838-40486208 | Common:1; Rare:74 | ||||
| chr17:40493216-40493455 | Common:2; Rare:36 | ||||
| chr17:40495551-40495653 | Common:3; Rare:9 | ||||
| chr17:40500781-40500890 | Common:1; Rare:25 | ||||
| chr17:40516795-40517031 | Common:1; Rare:35 | ||||
| chr17:40518597-40518926 | Common:3; Rare:68 | ||||
| chr17:40642516-40642711 | Rare:33; Clinvar:1; Clinvar (benign):1 |