| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:65133789-65133879 | Common:1; Rare:28 | ||||
| chr15:65185076-65185206 | Rare:74 | ||||
| chr15:65286841-65287087 | Rare:73 | ||||
| chr15:65517458-65517619 | Common:1; Rare:52 | ||||
| chr15:65611066-65611432 | Common:3; Rare:123 | ||||
| chr15:65792055-65792471 | Common:3; Rare:119 | ||||
| chr15:65869416-65869610 | Rare:76 | ||||
| chr15:65869864-65870031 | Common:1; Rare:45 | ||||
| chr15:66386676-66387355 | Common:6; Rare:217; Clinvar:4; Clinvar (benign):9 | ||||
| chr15:66500527-66500837 | Common:2; Rare:68 | ||||
| chr15:66501874-66501960 | Rare:26 | ||||
| chr15:66504772-66505368 | Common:4; Rare:233 | ||||
| chr15:66565903-66566055 | Rare:39 | ||||
| chr15:67065336-67065650 | Common:2; Rare:113 | ||||
| chr15:67066197-67066363 | Rare:34; Clinvar:3; Clinvar (benign):3 |