| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76103677-76103867 | Common:5; Rare:68 | ||||
| chr17:76353585-76353675 | Rare:39 | ||||
| chr17:76501355-76501580 | Rare:72; Clinvar (benign):3 | ||||
| chr17:76726443-76726898 | Common:5; Rare:174 | ||||
| chr17:76737309-76737485 | Common:3; Rare:71 | ||||
| chr17:76737870-76738089 | Common:3; Rare:63 | ||||
| chr17:77088612-77088817 | Common:1; Rare:59 | ||||
| chr17:77127749-77127984 | Rare:41 | ||||
| chr17:77206702-77206751 | Rare:16 | ||||
| chr17:77287759-77287958 | Rare:22 | ||||
| chr17:78128710-78128888 | Common:7; Rare:46 | ||||
| chr17:78168455-78168635 | Rare:54 | ||||
| chr17:78187045-78187371 | Common:3; Rare:104 | ||||
| chr17:78378632-78378706 | Common:1; Rare:39 | ||||
| chr17:78840751-78841060 | Common:2; Rare:111 |