| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41810943-41811308 | Common:1; Rare:154 | ||||
| chr17:41812589-41813014 | Common:3; Rare:91; Clinvar:5 | ||||
| chr17:41930522-41930665 | Rare:36 | ||||
| chr17:41966509-41966890 | Common:3; Rare:119 | ||||
| chr17:42017143-42017492 | Rare:114 | ||||
| chr17:42194419-42194567 | Rare:31 | ||||
| chr17:42316982-42317153 | Common:2; Rare:25 | ||||
| chr17:42422840-42423385 | Common:2; Rare:177; Clinvar:5 | ||||
| chr17:42423493-42423514 | Rare:6 | ||||
| chr17:42458775-42458953 | Common:3; Rare:59 | ||||
| chr17:42536123-42536299 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr17:42577596-42577832 | Rare:111 | ||||
| chr17:42609251-42609779 | Common:9; Rare:216; Clinvar (benign):2 | ||||
| chr17:42659279-42659492 | Rare:69 | ||||
| chr17:42659680-42659751 | Rare:11 |