| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75205344-75205750 | Common:1; Rare:130 | ||||
| chr17:75261580-75261982 | Common:4; Rare:138; Clinvar (benign):4 | ||||
| chr17:75393754-75394064 | Common:1; Rare:67 | ||||
| chr17:75667120-75667399 | Common:4; Rare:97 | ||||
| chr17:75979091-75979477 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:76072326-76072413 | Rare:34 | ||||
| chr17:76103695-76103859 | Common:4; Rare:58 | ||||
| chr17:76384316-76384681 | Common:3; Rare:99 | ||||
| chr17:76726453-76726888 | Common:5; Rare:167 | ||||
| chr17:77319448-77319969 | Common:4; Rare:127; Clinvar:2; Clinvar (benign):4 | ||||
| chr17:78186995-78187380 | Common:3; Rare:136 | ||||
| chr17:78840758-78840994 | Common:2; Rare:87 | ||||
| chr17:80220309-80220452 | Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:81034824-81035151 | Common:2; Rare:124 | ||||
| chr17:81239036-81239384 | Common:4; Rare:113 |