| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96208248-96208429 | Rare:89 | ||||
| chr2:96208805-96208974 | Common:3; Rare:66 | ||||
| chr2:96265959-96266374 | Common:2; Rare:123; Clinvar:1 | ||||
| chr2:96305449-96305609 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96335713-96335812 | Common:1; Rare:32 | ||||
| chr2:96740039-96740340 | Common:5; Rare:69 | ||||
| chr2:96857888-96858250 | Common:2; Rare:133 | ||||
| chr2:96870819-96870850 | Rare:5 | ||||
| chr2:97094820-97094940 | Common:1; Rare:24 | ||||
| chr2:97113420-97113797 | Common:4; Rare:111 | ||||
| chr2:97645861-97646095 | Common:2; Rare:70 | ||||
| chr2:98346418-98346476 | Rare:20 | ||||
| chr2:98444776-98445057 | Common:1; Rare:107 | ||||
| chr2:98608406-98608659 | Common:1; Rare:112; Clinvar (benign):1 | ||||
| chr2:99141495-99141776 | Common:2; Rare:96 |