| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45490719-45490863 | Rare:50 | ||||
| chr17:45620232-45620364 | Rare:30 | ||||
| chr17:45894208-45894686 | Common:5; Rare:139; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:46225349-46225479 | Common:1; Rare:33 | ||||
| chr17:46579642-46579990 | Rare:31 | ||||
| chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189215-47189436 | Rare:60 | ||||
| chr17:47323861-47323995 | Common:2; Rare:48 | ||||
| chr17:47831513-47831689 | Rare:50 | ||||
| chr17:47941348-47941713 | Rare:99; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:48048014-48048391 | Common:1; Rare:105 | ||||
| chr17:48101273-48101631 | Common:3; Rare:101 | ||||
| chr17:48830907-48831059 | Common:3; Rare:43 | ||||
| chr17:48944773-48944847 | Rare:26 | ||||
| chr17:49677971-49678321 | Rare:88 |