| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32277806-32277986 | Common:1; Rare:43 | ||||
| chr2:32627908-32628119 | Rare:58 | ||||
| chr2:33599222-33599442 | Common:1; Rare:82 | ||||
| chr2:37084276-37084549 | Common:3; Rare:100 | ||||
| chr2:37156924-37157029 | Common:1; Rare:34 | ||||
| chr2:37231542-37231722 | Common:4; Rare:106; Clinvar (benign):3 | ||||
| chr2:37324738-37324915 | Common:1; Rare:71 | ||||
| chr2:37671593-37671788 | Common:3; Rare:87 | ||||
| chr2:38377243-38377524 | Common:2; Rare:109 | ||||
| chr2:38602892-38603187 | Common:4; Rare:116 | ||||
| chr2:38666048-38666131 | Rare:26 | ||||
| chr2:38751230-38751636 | Common:6; Rare:208 | ||||
| chr2:38875886-38876064 | Common:1; Rare:65 | ||||
| chr2:39437078-39437453 | Common:4; Rare:134 | ||||
| chr2:40452067-40452229 | Common:4; Rare:60 |