| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59014725-59014902 | Rare:40 | ||||
| chr17:59047724-59047899 | Rare:44 | ||||
| chr17:59064352-59064699 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:59093357-59093442 | Rare:10 | ||||
| chr17:59104337-59104606 | Rare:73 | ||||
| chr17:59140800-59140965 | Rare:25 | ||||
| chr17:59332974-59333015 | Common:1; Rare:17 | ||||
| chr17:59333023-59333611 | Common:7; Rare:117 | ||||
| chr17:59335624-59335926 | Rare:54 | ||||
| chr17:59361785-59361969 | Common:2; Rare:34 | ||||
| chr17:59378670-59378879 | Common:1; Rare:38 | ||||
| chr17:59403119-59403124 | |||||
| chr17:59425740-59425873 | Rare:23 | ||||
| chr17:59428088-59428206 | Rare:28 | ||||
| chr17:59665881-59666872 | Common:2; Rare:187 |