| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:28870262-28870469 | Rare:84 | ||||
| chr2:30146599-30147049 | Common:5; Rare:146 | ||||
| chr2:32010949-32011107 | Rare:45 | ||||
| chr2:32039753-32039906 | Rare:51 | ||||
| chr2:32063345-32063676 | Common:1; Rare:120; Clinvar:1 | ||||
| chr2:32165668-32165898 | Common:1; Rare:92 | ||||
| chr2:32627896-32628119 | Rare:60 | ||||
| chr2:33599225-33599363 | Rare:57 | ||||
| chr2:37084269-37084569 | Common:4; Rare:114 | ||||
| chr2:37196446-37196508 | Rare:17 | ||||
| chr2:37231559-37231708 | Common:4; Rare:84; Clinvar (benign):3 | ||||
| chr2:37344569-37344738 | Common:1; Rare:63 | ||||
| chr2:37925249-37925538 | Common:3; Rare:122 | ||||
| chr2:38377233-38377519 | Common:2; Rare:116 | ||||
| chr2:38602895-38603070 | Common:3; Rare:76 |