| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7688188-7688486 | Common:5; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:7717662-7717794 | Rare:28 | ||||
| chr17:7843484-7843740 | Rare:86 | ||||
| chr17:7843953-7844106 | Common:2; Rare:46 | ||||
| chr17:7857100-7857321 | Common:1; Rare:112 | ||||
| chr17:7857472-7857656 | Common:1; Rare:61 | ||||
| chr17:7857854-7858100 | Rare:88 | ||||
| chr17:7885181-7885629 | Rare:103 | ||||
| chr17:7931890-7932273 | Common:5; Rare:105 | ||||
| chr17:8151166-8151416 | Common:1; Rare:62 | ||||
| chr17:8152352-8152583 | Common:2; Rare:55 | ||||
| chr17:8156298-8156695 | Common:2; Rare:119 | ||||
| chr17:8162881-8163093 | Common:1; Rare:75 | ||||
| chr17:8176313-8176483 | Rare:53 | ||||
| chr17:8248035-8248149 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):2 |