| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59693656-59693821 | Rare:47; Clinvar (pathogenic):1 | ||||
| chr17:59829258-59829548 | Common:1; Rare:38 | ||||
| chr17:59842635-59842873 | Rare:34 | ||||
| chr17:61089155-61089210 | Rare:5 | ||||
| chr17:61135970-61136128 | Common:1; Rare:39 | ||||
| chr17:61208688-61208831 | Rare:26 | ||||
| chr17:61396299-61396497 | Rare:51 | ||||
| chr17:61398117-61398349 | Common:4; Rare:48 | ||||
| chr17:63820105-63820253 | Common:4; Rare:65 | ||||
| chr17:64145765-64145975 | Common:2; Rare:54 | ||||
| chr17:64146283-64146357 | Common:1; Rare:36 | ||||
| chr17:64781484-64781660 | Common:2; Rare:40 | ||||
| chr17:64784031-64784130 | Rare:11 | ||||
| chr17:64837076-64837272 | Common:2; Rare:54 | ||||
| chr17:64975045-64975133 | Rare:19 |