| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41966444-41966882 | Common:3; Rare:130 | ||||
| chr17:42017149-42017511 | Common:1; Rare:118 | ||||
| chr17:42017524-42017657 | Rare:41 | ||||
| chr17:42019977-42020200 | Common:1; Rare:68 | ||||
| chr17:42120968-42121195 | Rare:57 | ||||
| chr17:42154893-42155196 | Common:3; Rare:80 | ||||
| chr17:42194408-42194551 | Rare:27 | ||||
| chr17:42317033-42317163 | Common:3; Rare:20; Clinvar (benign):1 | ||||
| chr17:42388297-42388525 | Rare:65; Clinvar:4 | ||||
| chr17:42422840-42423342 | Common:1; Rare:167; Clinvar:5 | ||||
| chr17:42423491-42423514 | Rare:6 | ||||
| chr17:42535923-42536275 | Common:3; Rare:96; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:42566974-42567305 | Common:4; Rare:103 | ||||
| chr17:42577631-42577844 | Rare:101 | ||||
| chr17:42609255-42609774 | Common:9; Rare:215; Clinvar (benign):2 |