| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76537877-76537941 | Rare:17 | ||||
| chr17:76540918-76541125 | Common:1; Rare:47 | ||||
| chr17:76550936-76551007 | Rare:14 | ||||
| chr17:76725969-76726085 | Common:1; Rare:29 | ||||
| chr17:76726454-76727187 | Common:7; Rare:293 | ||||
| chr17:76732910-76733037 | Rare:41; Clinvar (benign):1 | ||||
| chr17:76737309-76737591 | Common:3; Rare:104 | ||||
| chr17:76737845-76738089 | Common:3; Rare:70 | ||||
| chr17:76872524-76872905 | Common:1; Rare:104 | ||||
| chr17:77088591-77088783 | Common:1; Rare:52 | ||||
| chr17:77140591-77141045 | Common:5; Rare:162 | ||||
| chr17:77319394-77319433 | Rare:9 | ||||
| chr17:77319435-77319685 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:77319853-77319985 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:77320068-77320340 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 |