| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75231576-75231843 | Common:4; Rare:78 | ||||
| chr17:75232851-75233140 | Common:1; Rare:113 | ||||
| chr17:75234510-75234720 | Common:3; Rare:56 | ||||
| chr17:75261556-75262015 | Common:12; Rare:171; Clinvar (benign):4 | ||||
| chr17:75270298-75270357 | Common:1; Rare:13 | ||||
| chr17:75271107-75271369 | Common:2; Rare:54 | ||||
| chr17:75393679-75394064 | Common:1; Rare:95 | ||||
| chr17:75515466-75515631 | Common:3; Rare:50 | ||||
| chr17:75525486-75525807 | Common:3; Rare:103 | ||||
| chr17:75610552-75610947 | Common:3; Rare:77 | ||||
| chr17:75620321-75620489 | Common:3; Rare:43 | ||||
| chr17:75646103-75646376 | Common:5; Rare:58 | ||||
| chr17:75667108-75667474 | Common:5; Rare:125 | ||||
| chr17:75765128-75765279 | Common:1; Rare:48; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:75779062-75779461 | Common:2; Rare:184 |