| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80035855-80036031 | Common:1; Rare:62 | ||||
| chr17:80220309-80220475 | Common:1; Rare:63; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415387-80415492 | Common:4; Rare:40 | ||||
| chr17:80991806-80991933 | Common:1; Rare:51 | ||||
| chr17:81239036-81239317 | Common:2; Rare:92 | ||||
| chr17:81666244-81666336 | Rare:21 | ||||
| chr17:81666552-81666769 | Common:1; Rare:96 | ||||
| chr17:81683688-81684057 | Common:4; Rare:186 | ||||
| chr17:81703286-81703530 | Common:2; Rare:72; Clinvar (benign):2 | ||||
| chr17:81833243-81833343 | Rare:42 | ||||
| chr17:81937180-81937406 | Rare:79 | ||||
| chr17:81977491-81977642 | Rare:50 | ||||
| chr17:82051619-82051940 | Common:2; Rare:93 | ||||
| chr17:82273357-82273766 | Common:1; Rare:146 | ||||
| chr17:82450716-82450985 | Common:3; Rare:100 |