| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:82257497-82257680 | Common:1; Rare:60 | ||||
| chr17:82259395-82259472 | Rare:18 | ||||
| chr17:82261834-82262034 | Common:2; Rare:48 | ||||
| chr17:82292766-82293016 | Common:4; Rare:69 | ||||
| chr17:82522072-82522291 | Common:3; Rare:37 | ||||
| chr17:82536233-82536391 | Common:1; Rare:34 | ||||
| chr17:82536495-82536724 | Common:1; Rare:46 | ||||
| chr17:82567956-82568125 | Rare:40 | ||||
| chr17:82623418-82623696 | Rare:49 | ||||
| chr17:82630762-82631269 | Common:4; Rare:116 | ||||
| chr17:82746657-82746734 | Rare:17 | ||||
| chr17:82786846-82786955 | Common:6; Rare:10 | ||||
| chr17:82807276-82807661 | Common:1; Rare:91; Clinvar (pathogenic):1 | ||||
| chr17:82845440-82845935 | Common:14; Rare:99 | ||||
| chr17:82845972-82846192 | Common:1; Rare:48 |