| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7558195-7558309 | Rare:22 | ||||
| chr17:7558674-7558783 | Rare:21 | ||||
| chr17:7561796-7561996 | Common:2; Rare:52 | ||||
| chr17:7579363-7579722 | Common:1; Rare:121 | ||||
| chr17:7583542-7583877 | Common:1; Rare:137; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7590087-7590380 | Rare:57 | ||||
| chr17:7627793-7627969 | Common:2; Rare:58 | ||||
| chr17:7676203-7676485 | Common:5; Rare:98; Clinvar:9; Clinvar (benign):37; Clinvar (pathogenic):1 | ||||
| chr17:7687417-7687511 | Rare:23; Clinvar:2 | ||||
| chr17:7857936-7858003 | Rare:30 | ||||
| chr17:7885187-7885562 | Rare:86 | ||||
| chr17:7931906-7932248 | Common:5; Rare:94 | ||||
| chr17:8147567-8147772 | Common:1; Rare:74 | ||||
| chr17:8148077-8148255 | Rare:59 | ||||
| chr17:8151174-8151475 | Common:3; Rare:73 |