| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:31532024-31532370 | Common:3; Rare:99 | ||||
| chr5:32173927-32174034 | Rare:31 | ||||
| chr5:32174218-32174428 | Common:2; Rare:77 | ||||
| chr5:33440588-33441122 | Common:7; Rare:147 | ||||
| chr5:34007946-34008214 | Common:3; Rare:101; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:34656144-34656484 | Common:3; Rare:87 | ||||
| chr5:34915462-34915737 | Common:1; Rare:68 | ||||
| chr5:34929537-34929904 | Rare:136 | ||||
| chr5:35230459-35230555 | Rare:17 | ||||
| chr5:35617779-35617928 | Rare:30 | ||||
| chr5:35856788-35857053 | Rare:56; Clinvar (benign):1 | ||||
| chr5:36151794-36152140 | Rare:84 | ||||
| chr5:36876636-36876915 | Common:1; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877063-36877162 | Rare:36; Clinvar:1 | ||||
| chr5:37371053-37371414 | Common:2; Rare:88 |