| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32165745-32165898 | Common:1; Rare:57 | ||||
| chr2:32628017-32628139 | Rare:40 | ||||
| chr2:33599217-33599396 | Rare:71 | ||||
| chr2:37084276-37084565 | Common:3; Rare:110 | ||||
| chr2:37231437-37231708 | Common:5; Rare:137; Clinvar (benign):3 | ||||
| chr2:37324698-37324911 | Common:1; Rare:82 | ||||
| chr2:37671624-37671773 | Common:2; Rare:68 | ||||
| chr2:37925426-37925538 | Rare:46 | ||||
| chr2:38076147-38076197 | Rare:8 | ||||
| chr2:38602855-38603163 | Common:4; Rare:126 | ||||
| chr2:38875877-38876082 | Common:2; Rare:76 | ||||
| chr2:39121001-39121067 | Rare:20 | ||||
| chr2:39437071-39437453 | Common:4; Rare:136 | ||||
| chr2:42169160-42169446 | Common:1; Rare:140 | ||||
| chr2:43226559-43226811 | Common:2; Rare:100 |