| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32627889-32628125 | Rare:65 | ||||
| chr2:36561459-36561849 | Common:3; Rare:84 | ||||
| chr2:36598132-36598284 | Common:15; Rare:66 | ||||
| chr2:37084312-37084563 | Common:3; Rare:95 | ||||
| chr2:37156921-37157041 | Common:1; Rare:40 | ||||
| chr2:37196396-37196515 | Rare:39 | ||||
| chr2:37231559-37231714 | Common:4; Rare:86; Clinvar (benign):3 | ||||
| chr2:37344614-37344731 | Common:1; Rare:49 | ||||
| chr2:37671623-37671771 | Common:2; Rare:68 | ||||
| chr2:38602895-38603043 | Common:2; Rare:58 | ||||
| chr2:38875897-38876049 | Common:1; Rare:53 | ||||
| chr2:39437115-39437447 | Common:4; Rare:116 | ||||
| chr2:43595957-43596205 | Common:1; Rare:90 | ||||
| chr2:44361489-44361944 | Common:3; Rare:140 | ||||
| chr2:46073590-46073910 | Common:1; Rare:57 |