| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:20447279-20447670 | Common:3; Rare:111 | ||||
| chr2:20651050-20651276 | Rare:73 | ||||
| chr2:20823035-20823171 | Rare:51 | ||||
| chr2:23927057-23927330 | Common:3; Rare:95 | ||||
| chr2:23940388-23940553 | Common:3; Rare:60 | ||||
| chr2:24047359-24047625 | Common:1; Rare:69 | ||||
| chr2:24076219-24076551 | Rare:90 | ||||
| chr2:24084835-24085037 | Common:2; Rare:26 | ||||
| chr2:24123272-24123510 | Common:1; Rare:63 | ||||
| chr2:24360414-24360668 | Common:3; Rare:88 | ||||
| chr2:24793073-24793168 | Rare:49 | ||||
| chr2:24971906-24972170 | Common:1; Rare:82 | ||||
| chr2:26033769-26034167 | Common:4; Rare:149 | ||||
| chr2:26034290-26034732 | Common:3; Rare:107 | ||||
| chr2:26244528-26244995 | Common:2; Rare:168; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 |