| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76353627-76353759 | Common:1; Rare:47 | ||||
| chr17:76353814-76354034 | Common:1; Rare:82 | ||||
| chr17:76354163-76354310 | Rare:32 | ||||
| chr17:76383223-76383262 | Rare:8 | ||||
| chr17:76383494-76383542 | Rare:14 | ||||
| chr17:76384376-76384715 | Common:4; Rare:88 | ||||
| chr17:76452619-76452782 | Common:1; Rare:43 | ||||
| chr17:76453105-76453271 | Rare:59 | ||||
| chr17:76500983-76501130 | Rare:23 | ||||
| chr17:76501153-76501194 | Rare:8 | ||||
| chr17:76501308-76501624 | Rare:87; Clinvar (benign):3 | ||||
| chr17:76540904-76541070 | Common:1; Rare:39 | ||||
| chr17:76585958-76586079 | Rare:19 | ||||
| chr17:76710921-76711104 | Common:3; Rare:56 | ||||
| chr17:76725927-76726170 | Common:1; Rare:63 |