| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32585989-32586106 | Common:1; Rare:44 | ||||
| chr5:33440606-33441116 | Common:7; Rare:143 | ||||
| chr5:33891980-33892233 | Rare:51 | ||||
| chr5:34008027-34008214 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656078-34656473 | Common:4; Rare:110 | ||||
| chr5:34839082-34839196 | Rare:40 | ||||
| chr5:34915462-34915745 | Common:1; Rare:69 | ||||
| chr5:35230339-35230382 | Rare:9 | ||||
| chr5:35230459-35230489 | Rare:4 | ||||
| chr5:35230518-35230804 | Common:1; Rare:60 | ||||
| chr5:35617706-35617989 | Common:1; Rare:66 | ||||
| chr5:35938661-35938870 | Rare:32 | ||||
| chr5:36151819-36152174 | Rare:99 | ||||
| chr5:36606400-36606675 | Rare:47 | ||||
| chr5:36607141-36607331 | Rare:33 |