| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1645693-1645815 | Common:1; Rare:37 | ||||
| chr17:1684798-1685038 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1716186-1716520 | Common:2; Rare:102 | ||||
| chr17:1829783-1830071 | Common:8; Rare:120 | ||||
| chr17:2303746-2303983 | Common:2; Rare:91 | ||||
| chr17:2336423-2336624 | Rare:72 | ||||
| chr17:3636241-3636505 | Common:4; Rare:74; Clinvar (benign):1 | ||||
| chr17:3636648-3636784 | Common:1; Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3668552-3668837 | Common:2; Rare:112 | ||||
| chr17:3723769-3723932 | Common:1; Rare:94 | ||||
| chr17:4143013-4143244 | Rare:75 | ||||
| chr17:4143597-4143777 | Common:5; Rare:108 | ||||
| chr17:4263943-4264042 | Rare:43 | ||||
| chr17:4704116-4704231 | Rare:65 | ||||
| chr17:4807008-4807192 | Common:4; Rare:62 |