| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7843933-7844204 | Common:4; Rare:81 | ||||
| chr17:7857170-7857363 | Common:1; Rare:104 | ||||
| chr17:7857467-7857679 | Common:2; Rare:70 | ||||
| chr17:7931906-7932268 | Common:5; Rare:103 | ||||
| chr17:8079782-8080236 | Common:3; Rare:182 | ||||
| chr17:8080279-8080498 | Common:2; Rare:64; Clinvar:1 | ||||
| chr17:8087299-8087466 | Common:1; Rare:44; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:8087477-8087596 | Rare:27; Clinvar:1 | ||||
| chr17:8103482-8103785 | Common:2; Rare:76; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:8147536-8147722 | Common:1; Rare:74 | ||||
| chr17:8147738-8148104 | Rare:115 | ||||
| chr17:8149448-8149823 | Common:2; Rare:154 | ||||
| chr17:8151883-8152118 | Common:1; Rare:52 | ||||
| chr17:8152331-8152695 | Common:4; Rare:88 | ||||
| chr17:8156600-8156869 | Common:2; Rare:77 |