| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7014501-7015171 | Common:22; Rare:664 | ||||
| chr17:7015190-7016048 | Common:7; Rare:305 | ||||
| chr17:7023551-7024253 | Common:7; Rare:857 | ||||
| chr17:7035315-7035715 | Common:2; Rare:96 | ||||
| chr17:7035720-7036240 | Common:6; Rare:478 | ||||
| chr17:7177400-7177706 | Common:2; Rare:139 | ||||
| chr17:7177678-7178402 | Common:1; Rare:180 | ||||
| chr17:7217441-7217951 | Common:7; Rare:286; Clinvar:12 | ||||
| chr17:7218987-7219387 | Common:5; Rare:70 | ||||
| chr17:7219660-7220110 | Common:22; Rare:640; Clinvar:38; Clinvar (benign):18; Clinvar (pathogenic):4 | ||||
| chr17:7221125-7221525 | Common:10; Rare:99; Clinvar (benign):1 | ||||
| chr17:7221662-7222062 | Common:3; Rare:112; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
| chr17:7224180-7224780 | Common:8; Rare:355; Clinvar:26; Clinvar (benign):40; Clinvar (pathogenic):10 | ||||
| chr17:7233712-7234230 | Rare:311 | ||||
| chr17:7234255-7234954 | Common:10; Rare:852 |