| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39933850-39934330 | Common:5; Rare:151; Clinvar (benign):2 | ||||
| chr15:39934610-39935030 | Common:3; Rare:89 | ||||
| chr15:40002396-40002611 | Common:1; Rare:25 | ||||
| chr15:40039088-40039376 | Common:1; Rare:107 | ||||
| chr15:40106473-40106873 | Common:4; Rare:88 | ||||
| chr15:40108840-40109250 | Common:1; Rare:96 | ||||
| chr15:40160899-40161139 | Common:3; Rare:58 | ||||
| chr15:40238960-40239300 | Common:1; Rare:64 | ||||
| chr15:40291238-40291826 | Common:11; Rare:357 | ||||
| chr15:40293890-40294280 | Rare:81 | ||||
| chr15:40358074-40358316 | Common:8; Rare:101 | ||||
| chr15:40382833-40383026 | Common:1; Rare:96 | ||||
| chr15:40405491-40405848 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr15:40439500-40439760 | Rare:46 | ||||
| chr15:40439833-40440119 | Common:1; Rare:67 |