| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:96336156-96336556 | Common:5; Rare:127 | ||||
| chr15:96336775-96337573 | Common:12; Rare:426; Clinvar (pathogenic):2 | ||||
| chr15:96339207-96339607 | Rare:139 | ||||
| chr15:96340721-96340917 | Rare:55 | ||||
| chr15:96340940-96341370 | Common:6; Rare:350 | ||||
| chr15:96343341-96343822 | Common:2; Rare:167 | ||||
| chr15:96345614-96345894 | Common:1; Rare:64 | ||||
| chr15:96348533-96348970 | Common:7; Rare:196 | ||||
| chr15:96350219-96350619 | Common:4; Rare:126 | ||||
| chr15:96354140-96355234 | Common:20; Rare:399 | ||||
| chr15:96356817-96357217 | Rare:183 | ||||
| chr15:96357267-96357407 | Common:3; Rare:44 | ||||
| chr15:96358070-96358490 | Common:2; Rare:73 | ||||
| chr15:96359429-96360643 | Common:12; Rare:379 | ||||
| chr15:96491313-96492150 | Common:22; Rare:375 |