| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:55750837-55751106 | Common:2; Rare:139 | ||||
| chr17:56593220-56593385 | Common:1; Rare:63 | ||||
| chr17:56593516-56593839 | Rare:125 | ||||
| chr17:56795262-56795613 | Common:1; Rare:61 | ||||
| chr17:56833756-56834218 | Common:9; Rare:271 | ||||
| chr17:56913884-56914207 | Common:1; Rare:147 | ||||
| chr17:57084953-57085349 | Common:2; Rare:256 | ||||
| chr17:57256110-57256757 | Common:4; Rare:194 | ||||
| chr17:57849995-57850304 | Common:2; Rare:187 | ||||
| chr17:57988127-57988541 | Common:10; Rare:223 | ||||
| chr17:58006351-58006728 | Common:2; Rare:140 | ||||
| chr17:58007031-58007447 | Common:2; Rare:265 | ||||
| chr17:58007601-58007810 | Rare:84 | ||||
| chr17:58083155-58083480 | Common:8; Rare:228 | ||||
| chr17:58219163-58219381 | Common:2; Rare:154; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):1 |