| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50197948-50198206 | Common:3; Rare:66; Clinvar (benign):6 | ||||
| chr17:50199554-50199994 | Common:7; Rare:152; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50201392-50201681 | Common:2; Rare:87; Clinvar:4; Clinvar (benign):4 | ||||
| chr17:50271281-50271488 | Common:1; Rare:26 | ||||
| chr17:50274295-50274504 | Rare:48 | ||||
| chr17:50345911-50346146 | Common:4; Rare:80 | ||||
| chr17:50373160-50373261 | Common:3; Rare:44 | ||||
| chr17:50719463-50719667 | Rare:80 | ||||
| chr17:51153293-51153644 | Common:1; Rare:91 | ||||
| chr17:51166372-51166548 | Common:2; Rare:42 | ||||
| chr17:51260011-51260148 | Rare:46 | ||||
| chr17:51260362-51260598 | Common:3; Rare:110 | ||||
| chr17:54968607-54968792 | Common:3; Rare:90 | ||||
| chr17:55751324-55751433 | Common:2; Rare:37 | ||||
| chr17:56914074-56914177 | Rare:20 |