| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:20225914-20226058 | Common:3; Rare:31 | ||||
| chr2:20350831-20351045 | Common:1; Rare:88 | ||||
| chr2:20446841-20447081 | Common:3; Rare:98 | ||||
| chr2:20651040-20651255 | Rare:67 | ||||
| chr2:20823055-20823171 | Rare:46 | ||||
| chr2:21043862-21044217 | Common:3; Rare:97; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:21123833-21123995 | Common:1; Rare:54 | ||||
| chr2:23927057-23927330 | Common:3; Rare:95 | ||||
| chr2:23940370-23940538 | Common:3; Rare:62 | ||||
| chr2:24047351-24047483 | Common:1; Rare:32 | ||||
| chr2:24076204-24076594 | Rare:106 | ||||
| chr2:24123272-24123501 | Common:1; Rare:60 | ||||
| chr2:24360449-24360600 | Common:2; Rare:59 | ||||
| chr2:24793063-24793175 | Rare:54 | ||||
| chr2:24971578-24971842 | Common:2; Rare:93 |