| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79009666-79010002 | Common:10; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:79024126-79024183 | Rare:7 | ||||
| chr17:79024198-79024279 | Rare:13 | ||||
| chr17:79024375-79024686 | Common:2; Rare:77 | ||||
| chr17:79074585-79075044 | Common:6; Rare:121 | ||||
| chr17:79777534-79778287 | Common:1; Rare:252 | ||||
| chr17:79796520-79796787 | Rare:82 | ||||
| chr17:79796822-79796964 | Rare:45 | ||||
| chr17:79796971-79797687 | Common:2; Rare:214 | ||||
| chr17:79797823-79797938 | Rare:24 | ||||
| chr17:79798362-79798597 | Common:1; Rare:39 | ||||
| chr17:79800926-79801145 | Rare:41 | ||||
| chr17:79801252-79801465 | Common:1; Rare:38 | ||||
| chr17:79801541-79801620 | Rare:7 | ||||
| chr17:79839366-79839789 | Common:1; Rare:111 |