| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64162852-64163285 | Common:5; Rare:145; Clinvar:7; Clinvar (benign):5 | ||||
| chr15:64356025-64356336 | Rare:89 | ||||
| chr15:64381329-64381547 | Common:1; Rare:64 | ||||
| chr15:64387614-64387990 | Common:3; Rare:137 | ||||
| chr15:64700028-64700302 | Rare:56 | ||||
| chr15:64700591-64700942 | Common:2; Rare:67 | ||||
| chr15:64703031-64703092 | Rare:20 | ||||
| chr15:64703097-64703287 | Common:1; Rare:69 | ||||
| chr15:64775207-64775604 | Common:2; Rare:92 | ||||
| chr15:64775845-64776177 | Common:1; Rare:82 | ||||
| chr15:64825569-64826244 | Common:3; Rare:117 | ||||
| chr15:64841753-64841960 | Common:1; Rare:59 | ||||
| chr15:64989778-64990092 | Common:4; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:65026990-65027174 | Rare:47; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:65133504-65133715 | Common:1; Rare:71 |