| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:20350828-20351058 | Common:1; Rare:94 | ||||
| chr2:20446827-20447120 | Common:4; Rare:127 | ||||
| chr2:20447295-20447499 | Common:2; Rare:72 | ||||
| chr2:20651027-20651262 | Rare:71 | ||||
| chr2:20823056-20823164 | Rare:42 | ||||
| chr2:23927058-23927325 | Common:3; Rare:92 | ||||
| chr2:23940385-23940537 | Common:3; Rare:58 | ||||
| chr2:24076226-24076902 | Common:3; Rare:143 | ||||
| chr2:24123307-24123522 | Common:1; Rare:60 | ||||
| chr2:24360423-24360658 | Common:3; Rare:84 | ||||
| chr2:24971902-24972145 | Common:1; Rare:78 | ||||
| chr2:25673459-25673733 | Common:1; Rare:100 | ||||
| chr2:25878349-25878650 | Common:1; Rare:85 | ||||
| chr2:26033776-26034151 | Common:4; Rare:136 | ||||
| chr2:26194568-26194897 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 |