| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:42798677-42798776 | Rare:28 | ||||
| chr17:42833378-42833588 | Common:1; Rare:68 | ||||
| chr17:42964428-42964537 | Rare:51 | ||||
| chr17:42998244-42998517 | Common:4; Rare:77 | ||||
| chr17:43125317-43125694 | Rare:96; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43170268-43170712 | Common:3; Rare:87 | ||||
| chr17:43170982-43171278 | Common:1; Rare:101 | ||||
| chr17:43211758-43211912 | Common:1; Rare:34 | ||||
| chr17:43661266-43661590 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:43778878-43779078 | Rare:47 | ||||
| chr17:44070620-44070947 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:44078806-44078944 | Common:1; Rare:38 | ||||
| chr17:44093459-44093612 | Common:1; Rare:59 | ||||
| chr17:44111237-44111430 | Rare:52 | ||||
| chr17:44123594-44123840 | Common:3; Rare:72 |