| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42154937-42155150 | Common:2; Rare:51 | ||||
| chr17:42194428-42194586 | Rare:30 | ||||
| chr17:42423227-42423397 | Common:1; Rare:47; Clinvar:1 | ||||
| chr17:42458738-42458945 | Common:3; Rare:79 | ||||
| chr17:42566994-42567258 | Common:4; Rare:83 | ||||
| chr17:42577671-42577864 | Common:1; Rare:96 | ||||
| chr17:42609333-42609740 | Common:8; Rare:170; Clinvar (benign):2 | ||||
| chr17:42659169-42659460 | Rare:90 | ||||
| chr17:42682472-42682574 | Rare:25 | ||||
| chr17:42760648-42760886 | Common:5; Rare:78 | ||||
| chr17:42761056-42761254 | Rare:54 | ||||
| chr17:42773369-42773475 | Rare:30 | ||||
| chr17:42798536-42798767 | Rare:80 | ||||
| chr17:42833328-42833522 | Rare:69 | ||||
| chr17:42964436-42964537 | Rare:49 |