| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:63189393-63189614 | Common:2; Rare:77 | ||||
| chr15:64095796-64096013 | Common:5; Rare:73 | ||||
| chr15:64703183-64703411 | Common:2; Rare:89 | ||||
| chr15:65185310-65185690 | Common:2; Rare:146 | ||||
| chr15:65611096-65611365 | Common:1; Rare:87 | ||||
| chr15:66504772-66505161 | Common:2; Rare:142 | ||||
| chr15:67254629-67254801 | Rare:62 | ||||
| chr15:69298830-69298957 | Common:3; Rare:25 | ||||
| chr15:69414209-69414384 | Rare:51 | ||||
| chr15:69452688-69452891 | Common:4; Rare:93 | ||||
| chr15:70763438-70763731 | Common:2; Rare:101 | ||||
| chr15:72118168-72118403 | Common:2; Rare:74 | ||||
| chr15:72231123-72231497 | Common:3; Rare:115 | ||||
| chr15:72375958-72376070 | Common:2; Rare:50; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72686111-72686222 | Common:2; Rare:42; Clinvar:2; Clinvar (benign):2 |