| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7580213-7580472 | Common:1; Rare:81 | ||||
| chr17:7583538-7583872 | Common:1; Rare:134; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584065-7584125 | Rare:16 | ||||
| chr17:7687545-7687602 | Rare:11 | ||||
| chr17:7857452-7857707 | Common:2; Rare:83 | ||||
| chr17:7857925-7858095 | Rare:63 | ||||
| chr17:7931898-7932259 | Common:5; Rare:100 | ||||
| chr17:8248050-8248182 | Common:3; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:8295358-8295556 | Common:1; Rare:53 | ||||
| chr17:10697503-10697653 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:10729756-10729822 | Rare:33 | ||||
| chr17:14069463-14069539 | Common:1; Rare:23; Clinvar (benign):2 | ||||
| chr17:15699643-15699763 | Common:1; Rare:34 | ||||
| chr17:15999504-15999865 | Common:3; Rare:184; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr17:18039136-18039412 | Common:3; Rare:71; Clinvar (benign):1 |