| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7583730-7583861 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:7857924-7858095 | Rare:64 | ||||
| chr17:7931912-7932280 | Common:5; Rare:101 | ||||
| chr17:8248034-8248197 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249199-8249319 | Common:1; Rare:35 | ||||
| chr17:8295357-8295538 | Common:1; Rare:46 | ||||
| chr17:8867643-8867756 | Rare:19 | ||||
| chr17:8965705-8965802 | Common:1; Rare:29 | ||||
| chr17:10697505-10697654 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:10729983-10730058 | Common:3; Rare:14 | ||||
| chr17:11997431-11997607 | Rare:60 | ||||
| chr17:13017662-13017777 | Common:1; Rare:49; Clinvar (benign):2 | ||||
| chr17:13018000-13018257 | Common:4; Rare:62 | ||||
| chr17:14069347-14069580 | Common:2; Rare:84; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:15999532-15999875 | Common:3; Rare:174; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):2 |