| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40405664-40405827 | Common:2; Rare:52; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:40569201-40569365 | Common:3; Rare:40 | ||||
| chr15:40695083-40695171 | Rare:23 | ||||
| chr15:40807053-40807119 | Rare:17 | ||||
| chr15:40807405-40807767 | Common:4; Rare:121 | ||||
| chr15:40844175-40844221 | Rare:16 | ||||
| chr15:40894361-40894544 | Rare:51 | ||||
| chr15:41115982-41116260 | Common:2; Rare:77 | ||||
| chr15:41230714-41230831 | Rare:37 | ||||
| chr15:41402431-41402554 | Common:4; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:41416998-41417225 | Common:1; Rare:97 | ||||
| chr15:41477385-41477478 | Common:1; Rare:21 | ||||
| chr15:41544243-41544359 | Rare:49 | ||||
| chr15:41621162-41621552 | Common:2; Rare:87 | ||||
| chr15:41660302-41660523 | Rare:71 |