| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39581638-39582038 | Common:6; Rare:148 | ||||
| chr15:40069215-40069364 | Common:1; Rare:36 | ||||
| chr15:40081728-40081953 | Common:1; Rare:56 | ||||
| chr15:40098839-40098969 | Common:1; Rare:33 | ||||
| chr15:40103607-40103902 | Common:1; Rare:63 | ||||
| chr15:40104860-40105100 | Common:3; Rare:66 | ||||
| chr15:40146032-40146432 | Common:5; Rare:81 | ||||
| chr15:40283341-40283481 | Rare:40 | ||||
| chr15:40323388-40323697 | Common:4; Rare:92 | ||||
| chr15:40368053-40368351 | Common:2; Rare:125 | ||||
| chr15:40379731-40380215 | Common:7; Rare:235 | ||||
| chr15:40430523-40430741 | Common:2; Rare:36 | ||||
| chr15:40471620-40472270 | Rare:197; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):8 | ||||
| chr15:40507135-40507288 | Rare:38 | ||||
| chr15:40511750-40512065 | Common:2; Rare:78 |