| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75261588-75261962 | Common:4; Rare:124; Clinvar (benign):3 | ||||
| chr17:75393824-75394070 | Common:1; Rare:59 | ||||
| chr17:75667136-75667399 | Common:4; Rare:90 | ||||
| chr17:75784601-75784868 | Common:2; Rare:113 | ||||
| chr17:75979103-75979283 | Rare:50; Clinvar:4 | ||||
| chr17:76501402-76501558 | Rare:50; Clinvar (benign):3 | ||||
| chr17:76726491-76726898 | Common:5; Rare:152 | ||||
| chr17:76737325-76737505 | Common:2; Rare:68 | ||||
| chr17:76737864-76738071 | Common:3; Rare:56 | ||||
| chr17:77320074-77320281 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78187045-78187364 | Common:3; Rare:100 | ||||
| chr17:79022444-79023043 | Common:6; Rare:106 | ||||
| chr17:79023308-79023413 | Common:1; Rare:22 | ||||
| chr17:79023896-79024318 | Common:3; Rare:90 | ||||
| chr17:80220314-80220453 | Rare:54; Clinvar:1 |