| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5486801-5486917 | Common:4; Rare:34 | ||||
| chr17:6444133-6444502 | Common:2; Rare:114 | ||||
| chr17:6640635-6641085 | Common:7; Rare:137 | ||||
| chr17:6651574-6651727 | Common:1; Rare:49 | ||||
| chr17:7012315-7012686 | Rare:128 | ||||
| chr17:7241409-7241592 | Rare:45 | ||||
| chr17:7242278-7242606 | Common:1; Rare:107 | ||||
| chr17:7251963-7252308 | Common:1; Rare:136 | ||||
| chr17:7281385-7281685 | Common:1; Rare:66 | ||||
| chr17:7307233-7307748 | Common:6; Rare:142 | ||||
| chr17:7352081-7352207 | Rare:37 | ||||
| chr17:7484231-7484379 | Common:1; Rare:62 | ||||
| chr17:7561799-7562008 | Common:2; Rare:55 | ||||
| chr17:7577054-7577487 | Common:1; Rare:104 | ||||
| chr17:7583736-7583865 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 |