| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77141097-77141392 | Common:3; Rare:60 | ||||
| chr17:77141620-77141716 | Rare:18 | ||||
| chr17:77206694-77206855 | Rare:41 | ||||
| chr17:77211247-77211382 | Common:3; Rare:29 | ||||
| chr17:77281234-77281512 | Common:4; Rare:116 | ||||
| chr17:77319345-77319617 | Common:3; Rare:74; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:77320083-77320333 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:77320594-77320875 | Common:1; Rare:66 | ||||
| chr17:77322456-77322662 | Rare:40 | ||||
| chr17:77372836-77373001 | Common:1; Rare:39 | ||||
| chr17:77373164-77373420 | Rare:91 | ||||
| chr17:77373762-77373840 | Rare:14 | ||||
| chr17:77374357-77374563 | Common:1; Rare:55 | ||||
| chr17:77451368-77451591 | Common:1; Rare:52 | ||||
| chr17:78040730-78040917 | Common:3; Rare:40 |