| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75764237-75764963 | Common:4; Rare:288 | ||||
| chr17:75765064-75765688 | Common:8; Rare:283; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr17:75778959-75780237 | Common:16; Rare:1955 | ||||
| chr17:75784512-75785350 | Common:36; Rare:1171 | ||||
| chr17:75785294-75786020 | Common:3; Rare:329 | ||||
| chr17:75786027-75786205 | Common:1; Rare:26 | ||||
| chr17:75786257-75786657 | Rare:89 | ||||
| chr17:75843477-75843959 | Common:8; Rare:331; Clinvar (pathogenic):5 | ||||
| chr17:75844010-75844372 | Common:11; Rare:588; Clinvar:19; Clinvar (benign):18 | ||||
| chr17:75844502-75844906 | Common:13; Rare:254; Clinvar:21; Clinvar (benign):6 | ||||
| chr17:75845020-75845800 | Common:7; Rare:165 | ||||
| chr17:75854505-75856358 | Common:30; Rare:1647 | ||||
| chr17:75856271-75856671 | Common:3; Rare:100 | ||||
| chr17:75878453-75878853 | Common:12; Rare:290 | ||||
| chr17:75896130-75897245 | Common:31; Rare:1061 |