| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42458722-42458960 | Common:3; Rare:88 | ||||
| chr17:42577663-42577844 | Rare:87 | ||||
| chr17:42609321-42609737 | Common:8; Rare:177; Clinvar (benign):2 | ||||
| chr17:42659263-42659410 | Rare:46 | ||||
| chr17:42676955-42677315 | Common:1; Rare:96 | ||||
| chr17:42761065-42761274 | Rare:58 | ||||
| chr17:42773375-42773484 | Rare:35 | ||||
| chr17:42798536-42798646 | Rare:42 | ||||
| chr17:42833361-42833501 | Rare:53 | ||||
| chr17:42900532-42900834 | Common:1; Rare:52; Clinvar (benign):1 | ||||
| chr17:42964422-42964536 | Rare:53 | ||||
| chr17:43125317-43125723 | Rare:103; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170284-43170720 | Common:3; Rare:86 | ||||
| chr17:43171024-43171288 | Common:1; Rare:88 | ||||
| chr17:43211758-43211903 | Common:1; Rare:32 |