| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64990281-64990320 | Rare:4 | ||||
| chr15:65028968-65029190 | Common:3; Rare:44 | ||||
| chr15:65029441-65029707 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:65067972-65068195 | Common:1; Rare:51 | ||||
| chr15:65068277-65068479 | Common:1; Rare:30 | ||||
| chr15:65133754-65133995 | Common:1; Rare:71 | ||||
| chr15:65184448-65184619 | Rare:46 | ||||
| chr15:65184709-65185175 | Common:5; Rare:149 | ||||
| chr15:65185279-65185624 | Common:2; Rare:139 | ||||
| chr15:65286435-65286462 | Rare:9 | ||||
| chr15:65286678-65286930 | Common:1; Rare:75 | ||||
| chr15:65286944-65287140 | Rare:57 | ||||
| chr15:65385731-65385804 | Common:1; Rare:20 | ||||
| chr15:65423054-65423073 | Rare:6 | ||||
| chr15:65517144-65517201 | Rare:7 |