| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28336701-28336802 | Rare:18 | ||||
| chr17:28357113-28357271 | Common:2; Rare:39 | ||||
| chr17:28357405-28357783 | Common:7; Rare:178; Clinvar (pathogenic):2 | ||||
| chr17:28368235-28368536 | Common:1; Rare:61 | ||||
| chr17:28370218-28370641 | Common:3; Rare:81 | ||||
| chr17:28371328-28371561 | Common:2; Rare:46 | ||||
| chr17:28371806-28372084 | Rare:58 | ||||
| chr17:28384482-28384908 | Rare:130 | ||||
| chr17:28385053-28385237 | Rare:62 | ||||
| chr17:28385241-28385406 | Common:1; Rare:39 | ||||
| chr17:28405735-28405996 | Rare:65; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr17:28406104-28406455 | Common:1; Rare:78; Clinvar:1 | ||||
| chr17:28406560-28406686 | Common:2; Rare:21 | ||||
| chr17:28407202-28407374 | Common:2; Rare:32 | ||||
| chr17:28552547-28552739 | Rare:73; Clinvar:3; Clinvar (benign):1 |