| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42422612-42422752 | Rare:59; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr17:42574152-42574322 | Common:1; Rare:56; Clinvar:1 | ||||
| chr17:42680559-42680724 | Rare:47 | ||||
| chr17:43305983-43306083 | Rare:12 | ||||
| chr17:43315611-43315916 | Common:7; Rare:128 | ||||
| chr17:43388301-43388403 | Rare:19 | ||||
| chr17:43690751-43690905 | Common:1; Rare:24 | ||||
| chr17:43710256-43710436 | Common:2; Rare:35 | ||||
| chr17:43888414-43888615 | Common:1; Rare:31 | ||||
| chr17:43927384-43927611 | Common:1; Rare:46 | ||||
| chr17:43938179-43938296 | Common:1; Rare:36 | ||||
| chr17:44087601-44087771 | Common:1; Rare:47 | ||||
| chr17:44200960-44201234 | Common:1; Rare:45 | ||||
| chr17:44369702-44369793 | Rare:21 | ||||
| chr17:44669150-44669473 | Rare:59 |