| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:40771017-40771434 | Common:3; Rare:137 | ||||
| chr13:40789322-40789637 | Common:2; Rare:108; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:40789663-40789762 | Common:1; Rare:24 | ||||
| chr13:40982005-40982131 | Rare:30 | ||||
| chr13:40982864-40983052 | Common:3; Rare:32 | ||||
| chr13:41019290-41019368 | Rare:11 | ||||
| chr13:41060328-41060596 | Common:1; Rare:105 | ||||
| chr13:41060609-41060647 | Rare:6 | ||||
| chr13:41132479-41132559 | Common:1; Rare:30 | ||||
| chr13:41132592-41133050 | Common:2; Rare:118 | ||||
| chr13:41194231-41194750 | Common:2; Rare:129 | ||||
| chr13:41263302-41263350 | Rare:13 | ||||
| chr13:41263465-41263612 | Rare:37 | ||||
| chr13:41311185-41311317 | Rare:57 | ||||
| chr13:41311322-41311359 | Common:1; Rare:11 |