| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2303461-2303633 | Rare:63 | ||||
| chr17:2303728-2303983 | Common:2; Rare:97 | ||||
| chr17:2336430-2336553 | Rare:46 | ||||
| chr17:2511779-2512017 | Common:2; Rare:71 | ||||
| chr17:2593857-2593998 | Common:1; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:3557788-3557971 | Common:4; Rare:38; Clinvar:4; Clinvar (benign):5 | ||||
| chr17:3636241-3636482 | Common:4; Rare:64; Clinvar (benign):1 | ||||
| chr17:3668533-3668824 | Common:3; Rare:116 | ||||
| chr17:3723781-3723926 | Common:1; Rare:80 | ||||
| chr17:3801164-3801254 | Common:1; Rare:35 | ||||
| chr17:4142998-4143255 | Rare:85 | ||||
| chr17:4143597-4143740 | Common:4; Rare:80 | ||||
| chr17:4263942-4264099 | Rare:63 | ||||
| chr17:4555331-4555515 | Common:3; Rare:84 | ||||
| chr17:4704116-4704260 | Rare:76 |