| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42017379-42017584 | Common:1; Rare:78 | ||||
| chr17:42019985-42020124 | Common:1; Rare:43 | ||||
| chr17:42423248-42423453 | Common:1; Rare:53 | ||||
| chr17:42458719-42458914 | Common:1; Rare:74 | ||||
| chr17:42566957-42567113 | Common:3; Rare:53 | ||||
| chr17:42577671-42577869 | Common:1; Rare:102 | ||||
| chr17:42609326-42609723 | Common:8; Rare:169; Clinvar (benign):2 | ||||
| chr17:42773362-42773470 | Rare:29 | ||||
| chr17:42833378-42833456 | Rare:33 | ||||
| chr17:42964442-42964536 | Rare:43 | ||||
| chr17:42980453-42980562 | Common:1; Rare:39 | ||||
| chr17:43022376-43022494 | Rare:29 | ||||
| chr17:43125321-43125597 | Rare:65; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170325-43170479 | Common:2; Rare:31 | ||||
| chr17:43171063-43171236 | Rare:47 |