| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75710595-75711009 | Common:3; Rare:168 | ||||
| chr2:84459219-84459572 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84516282-84516546 | Common:1; Rare:71 | ||||
| chr2:84905464-84905896 | Common:2; Rare:131 | ||||
| chr2:85327910-85328084 | Common:2; Rare:82 | ||||
| chr2:85354501-85354790 | Common:1; Rare:97 | ||||
| chr2:85538675-85538842 | Common:2; Rare:50 | ||||
| chr2:85539068-85539353 | Common:3; Rare:145; Clinvar (benign):7 | ||||
| chr2:85561421-85561623 | Common:1; Rare:69; Clinvar:4 | ||||
| chr2:85577502-85577627 | Common:1; Rare:36 | ||||
| chr2:85595549-85595822 | Common:2; Rare:93 | ||||
| chr2:85602350-85602920 | Common:1; Rare:134 | ||||
| chr2:85612030-85612148 | Rare:28 | ||||
| chr2:85760473-85760793 | Rare:56 | ||||
| chr2:85888825-85889249 | Common:5; Rare:133; Clinvar:2; Clinvar (benign):3 |