| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58219231-58219348 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:58692541-58692668 | Common:1; Rare:70; Clinvar:10; Clinvar (benign):20 | ||||
| chr17:59106713-59106977 | Common:2; Rare:88; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59155408-59155770 | Rare:91 | ||||
| chr17:59565483-59565666 | Common:1; Rare:75 | ||||
| chr17:59619562-59619987 | Common:3; Rare:151 | ||||
| chr17:59685393-59685658 | Common:2; Rare:51 | ||||
| chr17:59707402-59707727 | Common:3; Rare:88; Clinvar (benign):2 | ||||
| chr17:59837595-59838084 | Common:1; Rare:70 | ||||
| chr17:59892846-59893170 | Common:1; Rare:96 | ||||
| chr17:59964708-59965044 | Common:2; Rare:99 | ||||
| chr17:60078910-60078988 | Common:4; Rare:41 | ||||
| chr17:60525927-60526004 | Common:2; Rare:22 | ||||
| chr17:60526147-60526290 | Rare:56 | ||||
| chr17:63550170-63550513 | Common:2; Rare:77 |