| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200963581-200963798 | Common:1; Rare:57 | ||||
| chr2:201071601-201072047 | Rare:96 | ||||
| chr2:201115727-201116215 | Common:2; Rare:102 | ||||
| chr2:201116229-201116454 | Rare:41 | ||||
| chr2:201118574-201118857 | Rare:47 | ||||
| chr2:201451416-201451826 | Common:2; Rare:110 | ||||
| chr2:201642643-201642735 | Rare:48 | ||||
| chr2:201643435-201643592 | Rare:41; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:202376071-202376518 | Rare:155 | ||||
| chr2:202911892-202912020 | Rare:28 | ||||
| chr2:202912127-202912298 | Common:2; Rare:57 | ||||
| chr2:202912474-202912583 | Common:2; Rare:36 | ||||
| chr2:203014672-203014931 | Common:1; Rare:78 | ||||
| chr2:203238937-203239030 | Rare:37 | ||||
| chr2:203239213-203239310 | Rare:30 |