| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45200489-45200656 | Common:1; Rare:47 | ||||
| chr15:45378481-45378743 | Common:4; Rare:69; Clinvar:2; Clinvar (benign):4 | ||||
| chr15:45587115-45587249 | Rare:22 | ||||
| chr15:45587288-45587586 | Common:1; Rare:104; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:45634668-45635103 | Common:1; Rare:113 | ||||
| chr15:48330960-48331153 | Common:3; Rare:43 | ||||
| chr15:48331316-48331457 | Common:3; Rare:49 | ||||
| chr15:48331854-48332344 | Common:7; Rare:160; Clinvar:1 | ||||
| chr15:48645697-48645989 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr15:48811029-48811152 | Common:1; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:48878004-48878325 | Rare:121 | ||||
| chr15:49155525-49155845 | Common:2; Rare:108 | ||||
| chr15:49620806-49621099 | Common:6; Rare:115 | ||||
| chr15:50113306-50113498 | Common:1; Rare:35 | ||||
| chr15:50354654-50355010 | Common:1; Rare:113 |