| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7583756-7583874 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:7584070-7584129 | Rare:11 | ||||
| chr17:7686418-7686677 | Rare:64 | ||||
| chr17:7843643-7843733 | Rare:32 | ||||
| chr17:7857383-7857735 | Common:3; Rare:113 | ||||
| chr17:7857869-7858074 | Rare:71 | ||||
| chr17:7885181-7885346 | Rare:47 | ||||
| chr17:7885519-7885723 | Common:1; Rare:52 | ||||
| chr17:7902987-7903350 | Common:2; Rare:84; Clinvar (pathogenic):1 | ||||
| chr17:7931866-7932235 | Common:5; Rare:97 | ||||
| chr17:8151247-8151491 | Common:2; Rare:54 | ||||
| chr17:8152378-8152707 | Common:4; Rare:79 | ||||
| chr17:8162936-8163093 | Rare:51 | ||||
| chr17:8176306-8176462 | Rare:50 | ||||
| chr17:8210555-8210744 | Common:2; Rare:33 |