| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:30146600-30147061 | Common:5; Rare:151 | ||||
| chr2:30147831-30147964 | Common:1; Rare:54 | ||||
| chr2:30231292-30231615 | Common:1; Rare:100 | ||||
| chr2:31233890-31234120 | Common:1; Rare:63 | ||||
| chr2:32009954-32010148 | Common:1; Rare:62 | ||||
| chr2:32039732-32039862 | Rare:39 | ||||
| chr2:32165745-32165898 | Common:1; Rare:57 | ||||
| chr2:32627918-32628139 | Rare:65 | ||||
| chr2:33134381-33134707 | Common:3; Rare:68 | ||||
| chr2:33599217-33599442 | Common:1; Rare:86 | ||||
| chr2:37084276-37084568 | Common:3; Rare:110 | ||||
| chr2:37156906-37157091 | Common:1; Rare:60 | ||||
| chr2:37231542-37231712 | Common:4; Rare:99; Clinvar (benign):3 | ||||
| chr2:37324713-37324911 | Common:1; Rare:78 | ||||
| chr2:37671431-37671782 | Common:2; Rare:125 |