| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42423127-42423422 | Common:1; Rare:77; Clinvar:2 | ||||
| chr17:42458724-42458924 | Common:2; Rare:75 | ||||
| chr17:42566926-42567149 | Common:3; Rare:80 | ||||
| chr17:42577630-42577869 | Common:1; Rare:119 | ||||
| chr17:42609333-42609745 | Common:8; Rare:172; Clinvar (benign):2 | ||||
| chr17:42682502-42682583 | Rare:20 | ||||
| chr17:42773362-42773495 | Rare:40 | ||||
| chr17:42780482-42780629 | Common:1; Rare:48 | ||||
| chr17:42798642-42798760 | Rare:39 | ||||
| chr17:42833351-42833539 | Rare:64 | ||||
| chr17:42964428-42964537 | Rare:51 | ||||
| chr17:42998073-42998682 | Common:5; Rare:143 | ||||
| chr17:43125313-43125654 | Rare:90; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170279-43170712 | Common:3; Rare:83 | ||||
| chr17:43171008-43171255 | Rare:82 |