| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7549006-7549118 | Common:1; Rare:23 | ||||
| chr17:7561784-7562131 | Common:3; Rare:93 | ||||
| chr17:7570421-7570791 | Rare:96 | ||||
| chr17:7577359-7577834 | Common:1; Rare:134 | ||||
| chr17:7579564-7579653 | Rare:25 | ||||
| chr17:7583496-7583886 | Common:1; Rare:156; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7584053-7584299 | Common:1; Rare:60 | ||||
| chr17:7627796-7627997 | Common:2; Rare:63 | ||||
| chr17:7687377-7687462 | Rare:17; Clinvar:3 | ||||
| chr17:7687467-7687649 | Rare:36 | ||||
| chr17:7857109-7857304 | Common:1; Rare:102 | ||||
| chr17:7857371-7857737 | Common:3; Rare:118 | ||||
| chr17:7857858-7858113 | Rare:93 | ||||
| chr17:7884605-7884882 | Common:1; Rare:29 | ||||
| chr17:7890285-7890960 | Common:1; Rare:167 |