| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75710601-75710782 | Common:2; Rare:69 | ||||
| chr2:75710864-75710975 | Common:1; Rare:44 | ||||
| chr2:84459172-84459599 | Common:3; Rare:116; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84881314-84881507 | Rare:29 | ||||
| chr2:84905552-84905730 | Common:1; Rare:50 | ||||
| chr2:84905732-84906148 | Common:1; Rare:111 | ||||
| chr2:84907006-84907326 | Rare:60 | ||||
| chr2:84970693-84970806 | Rare:35 | ||||
| chr2:85354524-85354813 | Common:1; Rare:95 | ||||
| chr2:85413970-85414117 | Common:1; Rare:33 | ||||
| chr2:85539024-85539373 | Common:3; Rare:167; Clinvar (benign):7 | ||||
| chr2:85540977-85541019 | Rare:9 | ||||
| chr2:85541042-85541109 | Rare:19; Clinvar (benign):1 | ||||
| chr2:85541725-85541871 | Common:2; Rare:45; Clinvar (benign):3 | ||||
| chr2:85561394-85561590 | Rare:73; Clinvar:5 |