| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24084215-24084453 | Common:5; Rare:111 | ||||
| chr2:24123264-24123506 | Common:1; Rare:63 | ||||
| chr2:24360315-24360639 | Common:4; Rare:100 | ||||
| chr2:24793097-24793171 | Rare:40 | ||||
| chr2:24971597-24971836 | Common:2; Rare:83 | ||||
| chr2:24971913-24972153 | Common:1; Rare:76 | ||||
| chr2:25878279-25878483 | Rare:48 | ||||
| chr2:25878485-25878756 | Common:3; Rare:87 | ||||
| chr2:25982469-25982609 | Rare:35 | ||||
| chr2:26033537-26033652 | Rare:24 | ||||
| chr2:26194568-26194848 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26244581-26244984 | Common:2; Rare:148; Clinvar:5; Clinvar (benign):9 | ||||
| chr2:26245168-26245215 | Rare:14 | ||||
| chr2:26345802-26346197 | Common:1; Rare:118 | ||||
| chr2:26764193-26764361 | Common:2; Rare:65 |