| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55051257-55051444 | Common:1; Rare:18 | ||||
| chr2:55232241-55232877 | Common:5; Rare:202 | ||||
| chr2:55269157-55269411 | Common:3; Rare:67 | ||||
| chr2:55419776-55420178 | Common:5; Rare:159 | ||||
| chr2:55519452-55519875 | Common:2; Rare:139 | ||||
| chr2:55618843-55618932 | Rare:25 | ||||
| chr2:55693781-55693983 | Common:1; Rare:71; Clinvar (benign):2 | ||||
| chr2:58046596-58046877 | Common:2; Rare:90 | ||||
| chr2:58047220-58047300 | Rare:26 | ||||
| chr2:58241216-58241431 | Rare:108; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:60550901-60551087 | Rare:48 | ||||
| chr2:60881401-60881687 | Common:2; Rare:91 | ||||
| chr2:61017171-61017309 | Common:3; Rare:38 | ||||
| chr2:61017420-61017756 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61065713-61065986 | Common:3; Rare:90 |