| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1361392-1361708 | Common:1; Rare:65 | ||||
| chr17:1400033-1400273 | Common:2; Rare:92 | ||||
| chr17:1456129-1456491 | Common:4; Rare:145 | ||||
| chr17:1491608-1491785 | Common:1; Rare:52 | ||||
| chr17:1516547-1517033 | Common:3; Rare:166 | ||||
| chr17:1648873-1649195 | Common:3; Rare:107 | ||||
| chr17:1684289-1684467 | Common:3; Rare:75 | ||||
| chr17:1684747-1685038 | Common:2; Rare:103; Clinvar:7; Clinvar (benign):1 | ||||
| chr17:1710334-1710463 | Rare:35 | ||||
| chr17:1716141-1716597 | Common:4; Rare:147 | ||||
| chr17:1829769-1830124 | Common:9; Rare:147 | ||||
| chr17:2303513-2303652 | Rare:48 | ||||
| chr17:2303733-2304007 | Common:2; Rare:102 | ||||
| chr17:2335669-2335970 | Rare:81 | ||||
| chr17:2336030-2336525 | Rare:197 |