| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24971902-24972213 | Common:1; Rare:100 | ||||
| chr2:26033792-26034131 | Common:3; Rare:116 | ||||
| chr2:26034535-26034681 | Rare:44 | ||||
| chr2:26244577-26244966 | Common:2; Rare:143; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345768-26346181 | Common:1; Rare:123 | ||||
| chr2:26764210-26764337 | Rare:52 | ||||
| chr2:27051472-27051669 | Rare:60 | ||||
| chr2:27211943-27212078 | Common:3; Rare:48 | ||||
| chr2:27212240-27212374 | Common:1; Rare:68 | ||||
| chr2:27323055-27323136 | Rare:19; Clinvar (benign):1 | ||||
| chr2:27356734-27357089 | Common:1; Rare:98 | ||||
| chr2:27370301-27370658 | Common:1; Rare:145 | ||||
| chr2:27442215-27442410 | Common:1; Rare:64 | ||||
| chr2:27489775-27490006 | Common:1; Rare:59 | ||||
| chr2:27628981-27629102 | Common:1; Rare:68 |