| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8076655-8077091 | Common:1; Rare:125; Clinvar:4; Clinvar (pathogenic):5 | ||||
| chr17:8104118-8104366 | Common:2; Rare:67; Clinvar:4 | ||||
| chr17:8110238-8110477 | Rare:97; Clinvar:1 | ||||
| chr17:8153375-8153675 | Rare:58 | ||||
| chr17:8153953-8154246 | Common:2; Rare:49 | ||||
| chr17:8154269-8154553 | Rare:62 | ||||
| chr17:8154733-8154824 | Rare:16 | ||||
| chr17:8154878-8155069 | Common:1; Rare:28 | ||||
| chr17:8155146-8155497 | Common:2; Rare:56 | ||||
| chr17:8190016-8190078 | Rare:16 | ||||
| chr17:8190136-8190299 | Rare:46 | ||||
| chr17:8476902-8477169 | Common:1; Rare:97 | ||||
| chr17:8477635-8477914 | Common:2; Rare:67 | ||||
| chr17:8478627-8478801 | Common:1; Rare:40 | ||||
| chr17:8491274-8491457 | Rare:34 |