| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44899383-44899750 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:45060987-45061339 | Common:2; Rare:93 | ||||
| chr17:45148165-45148603 | Common:1; Rare:153 | ||||
| chr17:46922858-46923189 | Common:4; Rare:92; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47323894-47323962 | Rare:21 | ||||
| chr17:47831516-47831641 | Rare:32 | ||||
| chr17:47941374-47941601 | Rare:46; Clinvar:1 | ||||
| chr17:48037683-48037845 | Common:4; Rare:39 | ||||
| chr17:48944773-48944918 | Common:2; Rare:47 | ||||
| chr17:49210591-49210712 | Rare:19 | ||||
| chr17:49788500-49788718 | Common:1; Rare:66 | ||||
| chr17:50188740-50189030 | Rare:73; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50189147-50189545 | Rare:87; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:50191948-50192035 | Rare:17; Clinvar (benign):2 | ||||
| chr17:50192473-50192705 | Common:1; Rare:54; Clinvar:4; Clinvar (benign):7 |