| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32010949-32011087 | Rare:36 | ||||
| chr2:32039761-32039860 | Rare:29 | ||||
| chr2:32165716-32165903 | Common:1; Rare:75 | ||||
| chr2:32277737-32278007 | Common:2; Rare:66 | ||||
| chr2:32627889-32628023 | Rare:31 | ||||
| chr2:32628031-32628123 | Rare:28 | ||||
| chr2:33457980-33458114 | Common:1; Rare:27 | ||||
| chr2:33476239-33476691 | Common:5; Rare:103 | ||||
| chr2:33599192-33599445 | Common:1; Rare:97 | ||||
| chr2:37084262-37084566 | Common:4; Rare:114 | ||||
| chr2:37156921-37157029 | Common:1; Rare:35 | ||||
| chr2:37196379-37196669 | Common:3; Rare:102 | ||||
| chr2:37231551-37231708 | Common:4; Rare:91; Clinvar (benign):3 | ||||
| chr2:37324695-37324911 | Common:1; Rare:82 | ||||
| chr2:37671501-37671823 | Common:10; Rare:126 |