| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76141243-76141396 | Common:1; Rare:45 | ||||
| chr17:76152375-76152628 | Common:1; Rare:75 | ||||
| chr17:76152951-76153040 | Common:1; Rare:16 | ||||
| chr17:76330593-76330719 | Common:1; Rare:23 | ||||
| chr17:76353579-76353671 | Rare:37 | ||||
| chr17:76353849-76354216 | Common:1; Rare:114 | ||||
| chr17:76501364-76501518 | Rare:53; Clinvar (benign):3 | ||||
| chr17:76570880-76571014 | Common:2; Rare:25 | ||||
| chr17:76688115-76688294 | Common:1; Rare:70 | ||||
| chr17:76688614-76688675 | Rare:10 | ||||
| chr17:76688677-76688710 | Common:1; Rare:7 | ||||
| chr17:76725948-76726149 | Common:1; Rare:53 | ||||
| chr17:76726449-76727049 | Common:5; Rare:234 | ||||
| chr17:76737251-76737591 | Common:4; Rare:149 | ||||
| chr17:76737845-76738158 | Common:4; Rare:87 |