| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75289387-75289759 | Common:2; Rare:109; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:75456463-75456656 | Rare:51 | ||||
| chr17:75667127-75667387 | Common:4; Rare:87 | ||||
| chr17:75784558-75784875 | Common:2; Rare:141 | ||||
| chr17:75844237-75844470 | Rare:73; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:75844492-75844645 | Common:2; Rare:30; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:75855295-75855658 | Common:1; Rare:98 | ||||
| chr17:75979096-75979490 | Common:1; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:76072372-76072529 | Common:6; Rare:111 | ||||
| chr17:76103708-76103880 | Common:5; Rare:56 | ||||
| chr17:76493130-76493482 | Common:1; Rare:65 | ||||
| chr17:76500981-76501056 | Rare:13 | ||||
| chr17:76501340-76501546 | Rare:66; Clinvar (benign):3 | ||||
| chr17:76726397-76726904 | Common:5; Rare:190 | ||||
| chr17:76737325-76737537 | Common:2; Rare:81 |