| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:21123855-21123985 | Common:1; Rare:43 | ||||
| chr2:23927073-23927301 | Common:3; Rare:83 | ||||
| chr2:24076242-24076594 | Rare:95 | ||||
| chr2:24123272-24123519 | Common:1; Rare:67 | ||||
| chr2:24793089-24793191 | Rare:55 | ||||
| chr2:24971907-24972153 | Common:1; Rare:79 | ||||
| chr2:26033771-26034124 | Common:4; Rare:125 | ||||
| chr2:26244585-26244975 | Common:2; Rare:143; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26345812-26346165 | Common:1; Rare:106 | ||||
| chr2:26764230-26764305 | Rare:25 | ||||
| chr2:27032871-27033004 | Rare:51 | ||||
| chr2:27071594-27071877 | Common:1; Rare:87 | ||||
| chr2:27212257-27212437 | Common:2; Rare:94 | ||||
| chr2:27282329-27282469 | Rare:21 | ||||
| chr2:27323050-27323136 | Rare:20; Clinvar (benign):1 |