| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79074631-79075045 | Common:5; Rare:110 | ||||
| chr17:80035843-80036031 | Common:1; Rare:66 | ||||
| chr17:80147041-80147360 | Common:5; Rare:134 | ||||
| chr17:80214628-80214934 | Common:1; Rare:98; Clinvar:3; Clinvar (pathogenic):3 | ||||
| chr17:80220309-80220453 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80384847-80385107 | Rare:62 | ||||
| chr17:80385288-80385606 | Common:1; Rare:89 | ||||
| chr17:80386553-80386733 | Rare:58 | ||||
| chr17:80415095-80415500 | Common:5; Rare:205 | ||||
| chr17:80991766-80991976 | Common:1; Rare:77 | ||||
| chr17:81034862-81035172 | Common:2; Rare:123 | ||||
| chr17:81239009-81239321 | Common:2; Rare:109 | ||||
| chr17:81247135-81247411 | Rare:78 | ||||
| chr17:81294860-81295047 | Common:2; Rare:48 | ||||
| chr17:81295197-81295424 | Common:2; Rare:54 |