| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64989670-64990180 | Common:15; Rare:423; Clinvar:9; Clinvar (benign):3 | ||||
| chr15:65029455-65029643 | Common:3; Rare:79; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:65133551-65134012 | Common:3; Rare:363 | ||||
| chr15:65184455-65184619 | Rare:71 | ||||
| chr15:65184782-65184933 | Rare:33 | ||||
| chr15:65185268-65185704 | Common:6; Rare:456 | ||||
| chr15:65285980-65286310 | Common:2; Rare:93 | ||||
| chr15:65286337-65286718 | Common:1; Rare:167 | ||||
| chr15:65286668-65287111 | Common:1; Rare:311 | ||||
| chr15:65377370-65377910 | Common:5; Rare:216 | ||||
| chr15:65377965-65378195 | Common:1; Rare:98 | ||||
| chr15:65516754-65517440 | Common:7; Rare:369 | ||||
| chr15:65517584-65517854 | Common:4; Rare:155 | ||||
| chr15:65530328-65530740 | Common:7; Rare:309 | ||||
| chr15:65530759-65531577 | Common:3; Rare:266 |