| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:33599210-33599469 | Common:1; Rare:97 | ||||
| chr2:37084262-37084434 | Common:4; Rare:53 | ||||
| chr2:37084452-37084561 | Rare:49 | ||||
| chr2:37231542-37231712 | Common:4; Rare:99; Clinvar (benign):3 | ||||
| chr2:37324695-37324963 | Common:1; Rare:105 | ||||
| chr2:38603018-38603180 | Common:3; Rare:62 | ||||
| chr2:38751242-38751491 | Common:2; Rare:143 | ||||
| chr2:38875908-38876036 | Common:1; Rare:38 | ||||
| chr2:39121022-39121146 | Rare:47 | ||||
| chr2:39124257-39124596 | Common:1; Rare:113 | ||||
| chr2:39437104-39437447 | Common:4; Rare:119 | ||||
| chr2:42169209-42169444 | Common:1; Rare:126 | ||||
| chr2:42568100-42568218 | Rare:34 | ||||
| chr2:43595957-43596205 | Common:1; Rare:90 | ||||
| chr2:43637145-43637308 | Common:2; Rare:60 |