| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79025330-79025645 | Common:5; Rare:53 | ||||
| chr17:80035843-80036037 | Common:1; Rare:68 | ||||
| chr17:80112621-80112914 | Common:2; Rare:119; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):7 | ||||
| chr17:80146999-80147365 | Common:8; Rare:153 | ||||
| chr17:80220309-80220488 | Common:1; Rare:65; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80372315-80372629 | Rare:81 | ||||
| chr17:80372824-80373165 | Common:2; Rare:117; Clinvar:1 | ||||
| chr17:80384825-80385091 | Rare:61 | ||||
| chr17:80415059-80415501 | Common:6; Rare:226 | ||||
| chr17:80991806-80991966 | Common:1; Rare:63 | ||||
| chr17:81239029-81239317 | Common:2; Rare:96 | ||||
| chr17:81295268-81295408 | Common:1; Rare:27 | ||||
| chr17:81512715-81513186 | Common:8; Rare:234; Clinvar (benign):14 | ||||
| chr17:81552175-81552487 | Common:1; Rare:102 | ||||
| chr17:81636947-81637246 | Common:3; Rare:121 |