| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63773527-63773852 | Common:2; Rare:107 | ||||
| chr17:65056600-65056887 | Common:3; Rare:113 | ||||
| chr17:68247907-68248119 | Common:5; Rare:89 | ||||
| chr17:68511812-68512042 | Rare:54 | ||||
| chr17:73232142-73232452 | Common:1; Rare:143 | ||||
| chr17:75012517-75012683 | Common:1; Rare:39 | ||||
| chr17:75109880-75109969 | Common:1; Rare:22 | ||||
| chr17:75261598-75261925 | Common:4; Rare:97; Clinvar (benign):1 | ||||
| chr17:75667179-75667364 | Common:4; Rare:56 | ||||
| chr17:75979146-75979271 | Rare:33; Clinvar:3 | ||||
| chr17:76103752-76103867 | Common:4; Rare:28 | ||||
| chr17:76726464-76726882 | Common:5; Rare:157 | ||||
| chr17:76737329-76737516 | Common:2; Rare:68 | ||||
| chr17:77320074-77320308 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78187069-78187362 | Common:3; Rare:86 |