| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24076205-24076862 | Common:2; Rare:147 | ||||
| chr2:24084820-24084959 | Common:2; Rare:20 | ||||
| chr2:24123272-24123526 | Common:1; Rare:68 | ||||
| chr2:24360315-24360675 | Common:4; Rare:107 | ||||
| chr2:24793052-24793175 | Rare:58 | ||||
| chr2:24971578-24971842 | Common:2; Rare:93 | ||||
| chr2:24971902-24972189 | Common:1; Rare:93 | ||||
| chr2:25878271-25878387 | Rare:25 | ||||
| chr2:25878428-25878657 | Common:1; Rare:63 | ||||
| chr2:26033782-26034151 | Common:3; Rare:132 | ||||
| chr2:26034310-26034544 | Common:3; Rare:56 | ||||
| chr2:26244528-26244839 | Common:2; Rare:119; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr2:26244858-26245118 | Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:26345758-26346165 | Common:2; Rare:123 | ||||
| chr2:26764210-26764325 | Rare:44 |