| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75667114-75667422 | Common:4; Rare:106 | ||||
| chr17:75764645-75764811 | Common:1; Rare:44 | ||||
| chr17:75765050-75765233 | Rare:63; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:75779414-75779574 | Common:1; Rare:78 | ||||
| chr17:75779691-75780189 | Common:2; Rare:189 | ||||
| chr17:75784492-75784922 | Common:2; Rare:195 | ||||
| chr17:75785013-75785419 | Common:2; Rare:104 | ||||
| chr17:75785872-75785929 | Rare:13 | ||||
| chr17:75843783-75843911 | Rare:33; Clinvar (pathogenic):1 | ||||
| chr17:75844291-75844532 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:75844534-75844674 | Common:2; Rare:24; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:75845212-75845580 | Common:4; Rare:72 | ||||
| chr17:75854824-75855095 | Common:2; Rare:46 | ||||
| chr17:75855230-75855780 | Common:2; Rare:154 | ||||
| chr17:75855898-75856191 | Common:3; Rare:63 |