| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:95165651-95165828 | Rare:54 | ||||
| chr2:95207439-95207604 | Rare:63 | ||||
| chr2:95402594-95402764 | Rare:57 | ||||
| chr2:96208250-96208418 | Rare:85 | ||||
| chr2:96208770-96208935 | Common:4; Rare:63 | ||||
| chr2:96265959-96266348 | Common:2; Rare:118; Clinvar:1 | ||||
| chr2:96305449-96305640 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96335716-96335812 | Common:1; Rare:30 | ||||
| chr2:96638292-96638445 | Common:1; Rare:39 | ||||
| chr2:96868525-96868758 | Rare:61 | ||||
| chr2:97094820-97094934 | Common:1; Rare:24 | ||||
| chr2:97113459-97113547 | Rare:20 | ||||
| chr2:97589825-97590023 | Common:4; Rare:43 | ||||
| chr2:97663902-97664247 | Common:1; Rare:110 | ||||
| chr2:98608406-98608636 | Common:1; Rare:100; Clinvar (benign):1 |