| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68512320-68512495 | Rare:58; Clinvar (benign):1 | ||||
| chr17:70169318-70169554 | Common:1; Rare:63 | ||||
| chr17:73232251-73232661 | Common:2; Rare:135 | ||||
| chr17:73311979-73312216 | Rare:62 | ||||
| chr17:74213276-74213580 | Common:4; Rare:64 | ||||
| chr17:74466545-74466741 | Rare:50 | ||||
| chr17:74545772-74545859 | Common:2; Rare:21 | ||||
| chr17:74545988-74546219 | Rare:36 | ||||
| chr17:74623614-74623941 | Common:1; Rare:73 | ||||
| chr17:74776166-74776502 | Common:4; Rare:97 | ||||
| chr17:75046943-75047201 | Common:1; Rare:76 | ||||
| chr17:75182942-75183213 | Common:1; Rare:86 | ||||
| chr17:75261568-75261980 | Common:4; Rare:146; Clinvar (benign):4 | ||||
| chr17:75270457-75270603 | Rare:24 | ||||
| chr17:75271146-75271386 | Common:3; Rare:44 |