| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58328780-58328944 | Common:1; Rare:47 | ||||
| chr17:58352113-58352495 | Common:6; Rare:143 | ||||
| chr17:58692559-58692709 | Common:1; Rare:79; Clinvar:21; Clinvar (benign):20 | ||||
| chr17:59106685-59107175 | Common:2; Rare:164; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:59154970-59155010 | Rare:20 | ||||
| chr17:59155153-59155517 | Common:2; Rare:79 | ||||
| chr17:59155557-59155784 | Rare:63 | ||||
| chr17:59220357-59220593 | Common:4; Rare:66 | ||||
| chr17:59565483-59565660 | Common:1; Rare:71 | ||||
| chr17:59619538-59619983 | Common:3; Rare:162 | ||||
| chr17:59707388-59707725 | Common:3; Rare:95; Clinvar (benign):4 | ||||
| chr17:59892884-59893149 | Rare:79 | ||||
| chr17:59964706-59965096 | Common:2; Rare:119 | ||||
| chr17:60078917-60078977 | Common:4; Rare:30 | ||||
| chr17:60526171-60526307 | Rare:55 |