| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:3636241-3636501 | Common:4; Rare:73; Clinvar (benign):1 | ||||
| chr17:3668552-3668845 | Common:2; Rare:117 | ||||
| chr17:3723764-3723925 | Common:1; Rare:89 | ||||
| chr17:4142985-4143250 | Rare:93 | ||||
| chr17:4143597-4143752 | Common:4; Rare:92 | ||||
| chr17:4263953-4264072 | Rare:46 | ||||
| chr17:4555312-4555514 | Common:3; Rare:93 | ||||
| chr17:4704116-4704245 | Rare:71 | ||||
| chr17:4731295-4731481 | Common:2; Rare:54 | ||||
| chr17:4806996-4807210 | Common:4; Rare:67 | ||||
| chr17:4833071-4833520 | Common:1; Rare:116 | ||||
| chr17:4899352-4899460 | Common:1; Rare:69; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:4939912-4940136 | Common:2; Rare:76 | ||||
| chr17:4948555-4948698 | Common:1; Rare:49 | ||||
| chr17:4948929-4949165 | Common:1; Rare:82 |