| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:20650997-20651236 | Rare:66 | ||||
| chr2:20823049-20823128 | Rare:35 | ||||
| chr2:21043862-21044227 | Common:4; Rare:100; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:23927056-23927325 | Common:3; Rare:92 | ||||
| chr2:23940388-23940514 | Common:3; Rare:47 | ||||
| chr2:24076205-24076747 | Common:1; Rare:135 | ||||
| chr2:24123272-24123506 | Common:1; Rare:62 | ||||
| chr2:24793006-24793111 | Rare:33 | ||||
| chr2:24793113-24793171 | Rare:31 | ||||
| chr2:24971902-24972145 | Common:1; Rare:78 | ||||
| chr2:25673459-25673722 | Common:1; Rare:96 | ||||
| chr2:25878438-25878672 | Common:1; Rare:66 | ||||
| chr2:26033778-26034203 | Common:3; Rare:153 | ||||
| chr2:26034320-26034733 | Common:3; Rare:101 | ||||
| chr2:26244530-26245039 | Common:2; Rare:174; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 |