| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10812704-10812796 | Rare:50 | ||||
| chr2:16665783-16665999 | Common:4; Rare:43 | ||||
| chr2:17753767-17753885 | Common:1; Rare:46 | ||||
| chr2:20051538-20051848 | Common:1; Rare:84 | ||||
| chr2:20446860-20447101 | Common:3; Rare:99 | ||||
| chr2:24076290-24076580 | Rare:72 | ||||
| chr2:24971964-24972138 | Common:1; Rare:51 | ||||
| chr2:26033792-26034189 | Common:3; Rare:141 | ||||
| chr2:26244579-26244969 | Common:2; Rare:143; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345773-26346152 | Common:1; Rare:111 | ||||
| chr2:27032862-27033018 | Rare:60 | ||||
| chr2:27212261-27212368 | Common:1; Rare:55 | ||||
| chr2:27356751-27356786 | Rare:4 | ||||
| chr2:27356973-27357088 | Common:1; Rare:40 | ||||
| chr2:27370324-27370680 | Common:2; Rare:142 |