| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:105361286-105361575 | Common:3; Rare:66; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:105610570-105610678 | Rare:22 | ||||
| chr2:105962349-105962409 | Rare:15 | ||||
| chr2:106110040-106110184 | Rare:31 | ||||
| chr2:106333557-106333829 | Common:1; Rare:62 | ||||
| chr2:107393094-107393206 | Rare:30 | ||||
| chr2:107468857-107469183 | Common:5; Rare:73 | ||||
| chr2:107542217-107542489 | Common:3; Rare:42 | ||||
| chr2:107542606-107542772 | Common:3; Rare:39 | ||||
| chr2:107746937-107747259 | Common:2; Rare:79 | ||||
| chr2:107753905-107754185 | Common:2; Rare:73 | ||||
| chr2:108217424-108217524 | Rare:16 | ||||
| chr2:108775434-108775936 | Common:2; Rare:128; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:109005920-109006103 | Common:1; Rare:52 | ||||
| chr2:109069905-109070059 | Rare:28 |