| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:30824135-30824252 | Rare:23 | ||||
| chr17:30824418-30824437 | Rare:7 | ||||
| chr17:30824488-30824977 | Common:4; Rare:169 | ||||
| chr17:30831882-30832018 | Rare:47 | ||||
| chr17:30832308-30832345 | Common:1; Rare:11 | ||||
| chr17:30906176-30906444 | Common:1; Rare:75 | ||||
| chr17:30906508-30906643 | Rare:18 | ||||
| chr17:30906722-30906857 | Common:1; Rare:19 | ||||
| chr17:30921769-30921973 | Rare:44 | ||||
| chr17:30970275-30970615 | Common:5; Rare:78 | ||||
| chr17:30970770-30971584 | Common:9; Rare:311; Clinvar (benign):2 | ||||
| chr17:31094562-31094604 | Rare:13 | ||||
| chr17:31094726-31095081 | Common:2; Rare:87; Clinvar:1 | ||||
| chr17:31095314-31095376 | Rare:10; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:31095394-31095525 | Rare:32; Clinvar (benign):1 |