| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41966610-41966885 | Common:1; Rare:99 | ||||
| chr17:42017382-42017506 | Common:1; Rare:53 | ||||
| chr17:42017516-42017537 | Rare:7 | ||||
| chr17:42017566-42017918 | Rare:97 | ||||
| chr17:42423137-42423390 | Common:1; Rare:67; Clinvar:2 | ||||
| chr17:42458749-42458914 | Common:1; Rare:64 | ||||
| chr17:42566980-42567159 | Common:3; Rare:58 | ||||
| chr17:42577651-42577864 | Common:1; Rare:103 | ||||
| chr17:42609333-42609752 | Common:8; Rare:173; Clinvar (benign):2 | ||||
| chr17:42761071-42761254 | Rare:52 | ||||
| chr17:42773371-42773495 | Rare:38 | ||||
| chr17:42780420-42780637 | Common:2; Rare:68 | ||||
| chr17:42833371-42833491 | Rare:49 | ||||
| chr17:42964428-42964536 | Rare:50 | ||||
| chr17:43125344-43125580 | Rare:46; Clinvar:3; Clinvar (benign):2 |