| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27663560-27663911 | Rare:126 | ||||
| chr2:27890394-27890788 | Rare:100 | ||||
| chr2:28751647-28752134 | Common:3; Rare:202 | ||||
| chr2:28870267-28870553 | Rare:101 | ||||
| chr2:30146600-30147050 | Common:5; Rare:146 | ||||
| chr2:32039761-32039851 | Rare:27 | ||||
| chr2:32165757-32165903 | Common:1; Rare:55 | ||||
| chr2:32627945-32628111 | Rare:53 | ||||
| chr2:33599275-33599438 | Common:1; Rare:50 | ||||
| chr2:37084262-37084544 | Common:4; Rare:100 | ||||
| chr2:37231557-37231696 | Common:4; Rare:75; Clinvar (benign):3 | ||||
| chr2:37671514-37671773 | Common:2; Rare:106 | ||||
| chr2:38076149-38076399 | Common:2; Rare:57 | ||||
| chr2:38751312-38751643 | Common:5; Rare:167 | ||||
| chr2:38875892-38876049 | Common:1; Rare:56 |