| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200888994-200889445 | Common:3; Rare:143 | ||||
| chr2:200963595-200963903 | Common:1; Rare:81 | ||||
| chr2:201071569-201072058 | Rare:111 | ||||
| chr2:201115949-201116436 | Common:2; Rare:90 | ||||
| chr2:201117435-201117586 | Rare:17 | ||||
| chr2:201118619-201118803 | Rare:27 | ||||
| chr2:201260473-201260573 | Rare:22 | ||||
| chr2:201451444-201451937 | Common:3; Rare:120 | ||||
| chr2:201642623-201642748 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr2:201780875-201781217 | Common:2; Rare:106; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238443-202238670 | Rare:79; Clinvar:1 | ||||
| chr2:202911441-202911769 | Rare:78 | ||||
| chr2:202912128-202912298 | Common:2; Rare:57 | ||||
| chr2:203014626-203014952 | Common:1; Rare:105 | ||||
| chr2:203238779-203239026 | Common:1; Rare:86 |