| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43517495-43517697 | Common:2; Rare:49 | ||||
| chr15:43746285-43746643 | Common:1; Rare:150 | ||||
| chr15:43777002-43777110 | Rare:32 | ||||
| chr15:43824490-43824811 | Common:2; Rare:96 | ||||
| chr15:44288386-44289009 | Common:39; Rare:294 | ||||
| chr15:44427551-44427746 | Common:1; Rare:51 | ||||
| chr15:44536672-44536784 | Rare:23 | ||||
| chr15:44536852-44537332 | Common:3; Rare:179 | ||||
| chr15:44663388-44663442 | Rare:20; Clinvar:2 | ||||
| chr15:44711312-44711635 | Rare:101; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44729365-44729534 | Common:1; Rare:40 | ||||
| chr15:45587199-45587651 | Common:1; Rare:140; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:45587691-45587848 | Common:2; Rare:44 | ||||
| chr15:45645755-45645974 | Rare:41 | ||||
| chr15:48149057-48149284 | Rare:52 |