| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:35578539-35578707 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chr17:35587184-35587586 | Rare:98 | ||||
| chr17:35795599-35795708 | Rare:26 | ||||
| chr17:35809149-35809580 | Common:1; Rare:159 | ||||
| chr17:36001342-36001425 | Common:1; Rare:20 | ||||
| chr17:36090137-36090354 | Common:1; Rare:39 | ||||
| chr17:36103819-36103832 | Rare:3 | ||||
| chr17:36534803-36535042 | Common:3; Rare:104 | ||||
| chr17:36544794-36544971 | Common:2; Rare:58 | ||||
| chr17:36545395-36545659 | Common:2; Rare:88 | ||||
| chr17:36601293-36601630 | Common:3; Rare:86 | ||||
| chr17:37406759-37406924 | Rare:70 | ||||
| chr17:37489678-37489915 | Rare:94 | ||||
| chr17:37609309-37609561 | Common:1; Rare:103 | ||||
| chr17:37745057-37745193 | Rare:34; Clinvar (benign):2 |