| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7857875-7858063 | Rare:64 | ||||
| chr17:7885182-7885346 | Rare:46 | ||||
| chr17:7931863-7932322 | Common:5; Rare:120 | ||||
| chr17:7937002-7937262 | Rare:60 | ||||
| chr17:8038912-8039139 | Common:3; Rare:62 | ||||
| chr17:8147474-8147794 | Common:1; Rare:116 | ||||
| chr17:8150979-8151028 | Rare:13 | ||||
| chr17:8152362-8152695 | Common:4; Rare:82 | ||||
| chr17:8156589-8156874 | Common:3; Rare:79 | ||||
| chr17:8162880-8163103 | Common:1; Rare:81 | ||||
| chr17:8176313-8176483 | Rare:53 | ||||
| chr17:8232466-8232562 | Rare:18 | ||||
| chr17:8248016-8248102 | Rare:52; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:8249024-8249331 | Common:1; Rare:69 | ||||
| chr17:8412967-8413204 | Common:4; Rare:43 |