| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42324797-42324932 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chr17:42423041-42423086 | Rare:18 | ||||
| chr17:42423093-42423310 | Rare:60; Clinvar:2 | ||||
| chr17:42458608-42458936 | Common:3; Rare:119 | ||||
| chr17:42566940-42567149 | Common:3; Rare:72 | ||||
| chr17:42577681-42577825 | Rare:65 | ||||
| chr17:42609320-42609723 | Common:8; Rare:170; Clinvar (benign):2 | ||||
| chr17:42760974-42761227 | Rare:62 | ||||
| chr17:42798661-42798760 | Rare:33 | ||||
| chr17:42833378-42833479 | Rare:41 | ||||
| chr17:42964428-42964528 | Rare:49 | ||||
| chr17:42980478-42980571 | Common:1; Rare:36 | ||||
| chr17:43017858-43018034 | Rare:47 | ||||
| chr17:43170297-43170517 | Common:2; Rare:43 | ||||
| chr17:43171035-43171278 | Common:1; Rare:79 |