| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96816473-96816662 | Rare:119 | ||||
| chr2:96857885-96858308 | Common:4; Rare:273 | ||||
| chr2:96868480-96868698 | Rare:95 | ||||
| chr2:96869397-96869577 | Common:4; Rare:89 | ||||
| chr2:96869906-96870620 | Common:3; Rare:191 | ||||
| chr2:97113069-97113262 | Rare:82 | ||||
| chr2:97113380-97113661 | Common:4; Rare:124 | ||||
| chr2:97589726-97589966 | Common:4; Rare:60 | ||||
| chr2:97645791-97646172 | Common:5; Rare:196 | ||||
| chr2:97663375-97663775 | Common:4; Rare:146 | ||||
| chr2:97663883-97664329 | Common:2; Rare:257 | ||||
| chr2:97712924-97713744 | Common:1; Rare:155; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:97995792-97996015 | Common:4; Rare:139 | ||||
| chr2:97996139-97996387 | Common:4; Rare:156 | ||||
| chr2:98444737-98444950 | Rare:177 |