| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:10696820-10697220 | Common:10; Rare:158 | ||||
| chr17:10697375-10697775 | Common:28; Rare:705; Clinvar:32; Clinvar (benign):25 | ||||
| chr17:10697900-10698010 | Common:2; Rare:23 | ||||
| chr17:10698095-10698773 | Common:6; Rare:167 | ||||
| chr17:11598270-11598530 | Common:4; Rare:72 | ||||
| chr17:11996610-11997010 | Common:3; Rare:87 | ||||
| chr17:11997261-11998068 | Common:27; Rare:1037 | ||||
| chr17:12020550-12020950 | Common:5; Rare:300 | ||||
| chr17:12021270-12021800 | Common:1; Rare:150 | ||||
| chr17:13017451-13017851 | Common:3; Rare:296; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:13017935-13018399 | Common:44; Rare:793; Clinvar (benign):10 | ||||
| chr17:13601390-13601790 | Common:2; Rare:112 | ||||
| chr17:13601760-13602410 | Common:16; Rare:491 | ||||
| chr17:14069300-14069680 | Common:14; Rare:632; Clinvar:22; Clinvar (benign):22; Clinvar (pathogenic):2 | ||||
| chr17:14069892-14070292 | Common:5; Rare:163 |