| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42609314-42609732 | Common:8; Rare:174; Clinvar (benign):2 | ||||
| chr17:42761083-42761254 | Rare:49 | ||||
| chr17:42773362-42773490 | Rare:38 | ||||
| chr17:42798654-42798744 | Rare:34 | ||||
| chr17:42833335-42833456 | Rare:47 | ||||
| chr17:42964214-42964537 | Common:5; Rare:137 | ||||
| chr17:42980385-42980579 | Common:1; Rare:60 | ||||
| chr17:42980806-42981024 | Rare:50 | ||||
| chr17:43125345-43125723 | Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170284-43170587 | Common:3; Rare:58 | ||||
| chr17:43171033-43171274 | Common:1; Rare:78 | ||||
| chr17:43545882-43546146 | Common:2; Rare:39 | ||||
| chr17:43778899-43779041 | Rare:32 | ||||
| chr17:44004367-44004634 | Rare:52 | ||||
| chr17:44005257-44005681 | Common:2; Rare:86 |