| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:67717838-67717959 | Rare:51 | ||||
| chr17:68247873-68248115 | Common:5; Rare:104 | ||||
| chr17:68291262-68291545 | Common:1; Rare:79 | ||||
| chr17:70169403-70169539 | Rare:37 | ||||
| chr17:72120793-72121028 | Rare:61 | ||||
| chr17:73192835-73193061 | Common:10; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:73232137-73232709 | Common:4; Rare:219 | ||||
| chr17:74213328-74213592 | Common:4; Rare:61 | ||||
| chr17:74431287-74431408 | Rare:29 | ||||
| chr17:74776323-74776506 | Common:4; Rare:52 | ||||
| chr17:75012610-75012696 | Rare:23 | ||||
| chr17:75261597-75261935 | Common:4; Rare:104; Clinvar (benign):2 | ||||
| chr17:75639946-75640224 | Common:1; Rare:74 | ||||
| chr17:75667131-75667396 | Common:4; Rare:92 | ||||
| chr17:75784589-75784868 | Common:2; Rare:119 |