| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42577682-42577844 | Rare:77 | ||||
| chr17:42609333-42609740 | Common:8; Rare:170; Clinvar (benign):2 | ||||
| chr17:42659340-42659396 | Rare:14 | ||||
| chr17:42675989-42676217 | Common:1; Rare:44 | ||||
| chr17:42761019-42761254 | Rare:66 | ||||
| chr17:42773362-42773484 | Rare:37 | ||||
| chr17:42833346-42833468 | Rare:47 | ||||
| chr17:42964427-42964528 | Rare:50 | ||||
| chr17:42998142-42998837 | Common:4; Rare:173 | ||||
| chr17:43125355-43125662 | Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:43170263-43170502 | Common:2; Rare:53 | ||||
| chr17:43171024-43171274 | Common:1; Rare:82 | ||||
| chr17:43545897-43546215 | Common:2; Rare:54 | ||||
| chr17:43778846-43779122 | Common:1; Rare:72 | ||||
| chr17:43833140-43833267 | Rare:34 |