| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27663555-27663924 | Rare:133 | ||||
| chr2:27890420-27890836 | Rare:108 | ||||
| chr2:28751497-28752134 | Common:4; Rare:256 | ||||
| chr2:28870270-28870429 | Rare:59 | ||||
| chr2:30146639-30147053 | Common:5; Rare:136 | ||||
| chr2:31234011-31234155 | Rare:38 | ||||
| chr2:32011006-32011105 | Rare:30 | ||||
| chr2:32039738-32039851 | Rare:35 | ||||
| chr2:32165752-32165898 | Common:1; Rare:54 | ||||
| chr2:32277788-32277972 | Common:1; Rare:45 | ||||
| chr2:32627945-32628125 | Rare:58 | ||||
| chr2:33599212-33599434 | Common:1; Rare:86 | ||||
| chr2:37084276-37084558 | Common:3; Rare:104 | ||||
| chr2:37231527-37231712 | Common:4; Rare:107; Clinvar (benign):3 | ||||
| chr2:37671588-37671740 | Common:1; Rare:74 |